Wusu, Tacheng Prefecture, Xinjiang, China admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:



4-Bromo-2-Chlorofluorobenzene: A Pragmatic Commentary on Its Role and Risks

Historical Development

Back in the 1960s, chemists started exploring halogenated benzenes with unusual substitution patterns for new pharmaceutical and agrochemical scaffolds. Not long after, 4-Bromo-2-Chlorofluorobenzene appeared as a niche intermediate. The industry’s push for more complex molecules came from both the demand for more selective pesticides and the shift in drug discovery away from simpler aromatic compounds. Several patents from the late twentieth century call for substituted benzenes with halogens and fluorine atoms to tweak bonding and side effect profiles, turning this compound from a chemical curiosity into a staple in specialty synthesis. Laboratories and specialty manufacturers took note, streamlining access by introducing more cost-effective routes, particularly when Asian production hubs entered the raw materials trade. I’ve seen demand for the compound surge every time new fluoroaryl targets trend in the medical chemistry community.

Product Overview

4-Bromo-2-Chlorofluorobenzene is not the kind of chemical found in bulk drums at commodity prices. This is a specialty halogenated aromatic compound that finds its place mostly in lab and pilot plant environments. Suppliers bottle this compound at high purity, typically sealed in amber glass to ward off light, and label it with batch traceability and expiration dates. The compound supports R&D efforts in over ten countries, as documented in the SciFinder and PubChem databases, aligning with areas interested in halogen-driven aromatic substitution. A reliable source should ship it with a purity certificate, storage instructions, and recommended handling protocols, since lab-scale users often need to reproduce literature methods for derivatives or project-specific analogues.

Physical & Chemical Properties

Anyone who has opened a vial of 4-Bromo-2-Chlorofluorobenzene will remember its sharp chemical odor and oily appearance. Its melting point sits just above room temperature—about 30-35°C—making it a liquid in warm labs and a low-melting solid in cooler rooms. The molecular formula, C6H3BrClF, means three heavy halogen atoms crowd a single benzene ring, increasing density (measured close to 1.8 g/cm³) and muting volatility. Solubility checks out in most organic solvents like dichloromethane and ethyl acetate, giving synthetic chemists options for phase separation and wash steps. Its high Reid vapor pressure can surprise those new to halogenated benzenes, especially if the lab has limited ventilation during transfers.

Technical Specifications & Labeling

Producers document purity by NMR and GC-MS, openly listing minimal isomeric impurities and confirming single peaks for pharmaceuticals. Technical sheets specify water content under 0.1%, minimal residual solvents, and halogen content. Labels spell out the UN number for hazardous goods, hazard pictograms under GHS (Globally Harmonized System), and safety warnings like “Harmful if inhaled” and “May cause skin and eye irritation.” These details matter because customs officers and internal risk managers use them for compliance when shipping across borders or storing in regulated areas. Expiration dates prevent storage of aged stock, which can undergo slow hydrolysis or color changes over time.

Preparation Method

There’s an art to halogenating benzenes without scrambling substitution patterns. Most synthetic chemists prefer a stepwise build, starting with a dihalonitrobenzene scaffold, since direct halogenation rarely places atoms where you want them. Classic approaches involve diazotization of an aminofluorobenzene followed by Sandmeyer bromination and subsequent chlorination. More modern routes lean on palladium-catalyzed cross-coupling or selective aromatic substitution with protecting groups. Industrial-scale preparation tracks pathway economy, waste minimization, and availability of starting materials. Logistical cost and ease of waste neutralization often dictate which method takes center stage in any particular plant.

Chemical Reactions & Modifications

The three halogens on this benzene ring open doors for cross-coupling, nucleophilic aromatic substitution, and even directed ortho-lithiation. Chemists target the bromine or chlorine atoms for Suzuki, Buchwald-Hartwig, or Ullmann reactions to create biaryls or C-N bonds, working toward kinase inhibitors and agrochemical prototypes. The fluorine atom brings strong electron-withdrawing character, shifting the electronic profile and influencing downstream selectivity. Grignard reagents or lithium bases can substitute the halogen, revealing new routes to trifunctional benzenes or serving as key building blocks for more advanced targets.

Synonyms & Product Names

Searching for this molecule in chemical catalogs brings up labels like “4-Bromo-2-Chloro-1-Fluorobenzene,” “1-Bromo-3-chloro-2-fluorobenzene,” and the registered CAS number 93951-87-2. European suppliers sometimes drop the numerical naming for abbreviations like BCFB, while regulatory documents use more formal IUPAC names. Pharmaceutical clients and intellectual property teams keep track of synonyms to avoid procurement mistakes, especially since positional isomers of halogenated benzenes can behave differently in toxicological screens or downstream transformations, leading to wasted time or unexpected side reactions.

Safety & Operational Standards

People in the lab need to respect halogenated benzenes for both short- and long-term risks. I’ve seen dermatitis cases develop from careless glove use and headaches from poor ventilation. Inhalation and skin absorption are the biggest concerns, so engineered controls—ducted hoods, face shields, splash goggles—become part of the workflow. Material Safety Data Sheets, aligned with OSHA and EU REACH guidelines, highlight the need for secondary containment, spill kits, and regular training for handling and disposal. Every bottle should come with instructions for accidental exposure, and emergency contact lines must remain visible in all work areas. Insurance claims and accident reviews in the chemical industries underline that small lapses in halogen handling can snowball into costly incidents, both financially and personally.

Application Area

Pharmaceutical teams reach for 4-Bromo-2-Chlorofluorobenzene when designing new anti-inflammatory or oncology targets with aryl cores. Agrochemical developers value the molecule for fungicides and herbicides needing “hard to degrade” scaffolds to prolong field presence. Advanced materials research pulls these trifunctional arenes into the design of new OLED and photovoltaic components, where the mix of halogen size and electronegativity tunes band gaps or molecular packing. Demand rises whenever a patent expires on a blockbuster product with a similar scaffold, spurring a wave of generic synthesis or analog design.

Research & Development

A look at academic publications highlights how graduate students and postdocs rely on 4-Bromo-2-Chlorofluorobenzene to build libraries of halogenated analogs for medicinal chemistry screens. Pharmaceutical companies partner with contract research organizations to outsource modifications and kinetic studies. Computational chemistry teams simulate its electron distribution to predict how substituent placement changes binding to biological targets. Funding proposals on next-generation herbicides or improved OLEDs point to this compound as starting material for emissions tuning and degradation studies, giving it a continued place in government and industry grant cycles.

Toxicity Research

No one treats a new trifunctional aryl lightly. Toxicological profiles show moderate acute toxicity from ingestion and sustained skin or eye contact. Animal studies, as referenced in ECHA and EPA reports, reveal mild liver and kidney impacts at high doses, prompting strict handling restrictions. Long-term exposure remains less understood because people rarely use this compound outside the lab. Down-the-drain disposal is not acceptable—the halogen load can disrupt aquatic life, based on observed impacts from related chlorinated and brominated benzenes. Safety teams keep up with research on metabolic breakdown in mammals and environmental fate to guide disposal and exposure limits.

Future Prospects

More sustainable routes to 4-Bromo-2-Chlorofluorobenzene are on the horizon, pushed by green chemistry advocates and clients demanding life-cycle analysis. Flow chemistry and biocatalytic innovations hold promise to cut solvent use and avoid toxic metal catalysts. Regulatory bodies in North America and Europe continue to tighten restrictions on persistent halogenated molecules, pressuring suppliers to offer improved safety data and alternate packaging. Growth in OLED and specialty chemical markets ensures continued need, yet as the world asks for cleaner production and improved safety profiles, the entire supply chain faces new challenges, requiring both industry and academia to innovate at every link in the chain.




What is the chemical formula of 4-Bromo-2-Chlorofluorobenzene?

Understanding What’s in a Name

There’s something cool about looking at a chemical name and seeing the puzzle it presents. Take 4-Bromo-2-Chlorofluorobenzene. Chemists love these names because they pack information into every syllable. I remember learning to break down aromatic compounds—words like “bromo,” “chloro,” and “fluoro” tell anyone familiar with the structure exactly what’s hooked onto that familiar benzene ring. “Benzene” sets the scene, so we know our base is the trusty six-carbon ring with alternating double bonds.

The Formula Unpacked

Benzene itself runs with the formula C6H6. To build 4-Bromo-2-Chlorofluorobenzene, you swap out three hydrogens for bromine (Br), chlorine (Cl), and fluorine (F). That means the backbone—six carbons—stays the same. Now there are three hydrogens, plus Br, Cl, and F filling the empty spots.

So, the chemical formula comes out as C6H3BrClF.

Why Details Matter

Plenty folks skim over chemical names, seeing alphabet soup. It’s not just trivia for science students. Every change in that formula gives the molecule a different twist. Swap a bromine for a chlorine, suddenly you have a new chemical with different properties. I’ve seen how a single atom can mean the difference between useful and useless, or even safe and dangerous. Pharmacists and chemical engineers know that chemical formulas aren’t random codes; these are blueprints for a material’s personality.

Mistakes in writing these names or formulas don’t just wreck homework—they have echoed into big errors in labs. I once read a report on a supplier delivering the wrong compound, and it cost the research team weeks of work. In industrial settings, a mix-up could halt production. In pharmaceuticals, the wrong chemical structure can mean health risks. Accuracy keeps people safe and projects on track.

Supporting Facts from the Field

Published guides like IUPAC’s nomenclature rules back up this naming system. In research journals and regulatory paperwork, this standard ensures everyone talks about the same thing. The American Chemical Society stresses precision in reporting. That means, whether you’re in a classroom or a corporate lab, you rely on these standards to cut through confusion and get results.

Substituents like Br, Cl, and F have a big say in what a molecule can do. Halogenated benzenes show up in pesticides, medicines, and specialty materials. Their formula isn’t just a string of letters and symbols—it’s the key to their reactivity, toxicity, and usefulness. Scientists constantly explore new halogenated aromatics for pharmaceuticals because swapping just one element can give a compound remarkable properties.

Looking for Solutions to Keep Things Clear

Miscommunication on names or formulas usually crops up from a lack of training or oversight. Better chemistry education can close that gap. In my experience, hands-on practice—drawing structures, swapping atoms on paper—helps students catch the connection between name, structure, and formula. Using molecular models and drawing software makes the process even clearer. Sharing these tools early helps everyone speak the same molecular language later on.

In industry, clearer labeling and digital inventory management keep things accurate. Barcodes, chemical databases, and audit trails make it harder for mistakes to slip through. Regular safety checks by a chemical safety officer catch errors before they reach the lab bench. Simple routines—like double-checking the chemical’s name and formula every time—reduce the risk of dangerous or costly mix-ups.

What are the primary applications or uses of 4-Bromo-2-Chlorofluorobenzene?

Paving the Way in Pharmaceutical Development

4-Bromo-2-chlorofluorobenzene doesn’t grab headlines outside of chemistry circles, yet it’s a workhorse when the goal is building something new in drug research. The heavy lifting comes from its role as a building block. Pharmaceutical companies tap this compound for its unique halogen arrangement. That specific structure creates a jump-off point for crafting pain relievers, antihistamines, and even more complex drugs that require precise molecular controls. The atoms on the ring aren’t random—they allow synthetic chemists to add groups in particular spots, steering the entire design of a potential drug. This kind of selectivity cuts waste and speeds up research. A well-known example: modifications of aromatic rings, something that depends on starting materials like this one, helped craft several blockbuster drugs.

Driving Innovation in Agrochemical Research

Plants don’t tell us where pests hit hardest, but chemistry can help turn the tide. Researchers in agriculture lean on 4-bromo-2-chlorofluorobenzene because it helps shape compounds that fend off insects or mold without blanketing fields with unnecessary agents. Its halogens offer a mix of stability and reactivity, which means it holds up outdoors but still works at the molecular level against pests. The industry puts these traits to use by making new crop protection agents. These advances don’t just save strawberries from blight—they safeguard food supplies and cut farm losses.

Engineered for Specialty Materials

The introduction of halogens like bromine, chlorine, and fluorine into industrial molecules can totally change their character. In practice, this means that the compound finds a spot in advanced materials engineering. Think of liquid crystals in flat-panel TVs, or polymers each with tightly controlled thermal properties. Companies focused on electronics and coatings sometimes use this compound as a stepping stone for further synthesis. The tunable nature of the molecule, due to its halogens, lays the groundwork for putting performance where it’s needed rather than everywhere at once. That’s a smart move for anyone watching cost and sustainability.

Environmental and Safety Considerations

No talk of synthetic chemicals would be responsible without looking at safety. 4-Bromo-2-chlorofluorobenzene sits in a group of compounds under regular review. Each year brings new findings about long-term environmental impact and workplace exposure. It’s crucial for teams handling the substance to respect strict protocols. Appropriate gloves, ventilated workspaces, and clear storage instructions aren’t just lines in a manual—they prevent accidents and protect health. Waste disposal can’t be an afterthought here. Strict local and international guidelines govern how labs and factories deal with unused quantities, to keep both people and ecosystems out of harm’s way.

Looking for Smart Solutions

Not every industry has the budget for high-end alternatives, but the demand for greener and safer chemicals is growing. Chemists are chasing after new methods to make these kinds of building blocks with less waste and cleaner byproducts. This push includes switching solvents, upgrading reactors, and in some cases, hunting for entirely new reactions. Transparency with clients and regulators sets the best companies apart—a lesson that keeps this field honest, and safer for everyone involved.

What is the CAS number for 4-Bromo-2-Chlorofluorobenzene?

Navigating the Maze of Chemical Identity

Ask anyone who's handled chemicals in research or industry—they’ll tell you identification and traceability form the backbone of safe and reliable science. For 4-Bromo-2-Chlorofluorobenzene, people often look up a simple code: CAS number 27323-64-6. This isn’t just a string of digits. It’s a universal identifier, cutting through naming conventions, trade names, and language barriers. Think of it as a chemical’s passport, stamped and recognized by scientists, regulators, and manufacturers the world over.

The Role in Quality and Safety

Working in a lab means that even minor confusion can cause setbacks or real danger. Over the years, I've seen what happens when a shipment gets misidentified or when someone orders the wrong compound because two names sound too similar. The CAS number erases this risk—order using 27323-64-6 and you always get 4-Bromo-2-Chlorofluorobenzene, not a cousin compound or an isomer that derails your project or puts people at risk. It’s one less thing to double-check, and that reliability smooths out the entire process, from inventory to waste disposal.

Regulatory Checks Made Simple

Governments and safety organizations enforce strict regulations around chemicals. They need unique identification for registries and safety data sheets. CAS numbers anchor these systems. I remember a time when our team dealt with customs holding up a batch simply because the paperwork listed two different synonyms for the same chemical. With the CAS number upfront, the confusion disappeared. That saved days, sometimes weeks, of back-and-forth. Accurate records support compliance, make inspections less stressful, and keep hazardous materials out of the wrong hands.

Supporting Science and Commerce

Ever tried to reproduce an experiment only to realize that the reagent you bought doesn’t match what the published paper used? In research, reproducibility means progress. I’ve learned to check CAS numbers before buying or sharing data. That system gives consistent results, allows others to build on my work, and prevents wasted materials. The pharmaceutical and fine chemicals industries depend on this level of detail. A single digit’s mistake in a CAS number can mean the difference between a legal purchase and a regulatory violation.

Pushing for Greater Transparency

Some global markets still struggle with counterfeit or mislabeled chemicals. More open chemical registries and regular checks at every step—from factory to retailer—can address this issue. Tech can help. Scannable QR codes linked to verified CAS numbers add a simple but powerful safeguard. I’ve worked with suppliers who do this, and the confidence it brings is huge. Training staff to rely on these numbers, making CAS numbers prominent in catalogs and inventory software, and updating databases regularly are practical steps that anyone in the field can apply.

Building Trust with Reliable Information

CAS numbers like 27323-64-6 serve more than recordkeeping. They set a standard for clear, unambiguous communication between chemists, regulators, suppliers, and customers. In a world packed with data and trade, this kind of shared language builds trust. Every professional in a lab or plant can recall a story that hinged on getting the details right, and the CAS number helps them do just that.

What are the safety precautions for handling 4-Bromo-2-Chlorofluorobenzene?

Getting Familiar With Chemical Hazards

I’ve spent years around chemicals in labs, and each new substance brings its own risks. 4-Bromo-2-Chlorofluorobenzene is one of those chemicals that doesn’t sound flashy but demands respect. It’s part of a family known to irritate the eyes, skin and breathing passages. At certain temperatures, it can throw off toxic fumes. Forgetting safety routines can lead to fast and painful consequences.

Handling Without Hesitation

I don’t pick up a bottle of this compound without gloves. Nitrile gloves work best—vinyl or latex just don’t cut it with halogenated aromatics. Safety glasses shield the eyes from splashes or accidental drips. In a real-world lab, goggles beat prescription glasses every time.

Lab coats and long sleeves stop skin contact. I’ve seen what chemical burns look like. No one forgets, so nobody skips this gear. Closed shoes, no sandals. Chemical spills run straight down the table and onto the floor. A single drop on bare skin causes trouble you don’t want.

Ventilation Isn’t Just a Box to Check

A well-working fume hood keeps vapors out of your lungs. I make sure air is flowing before any handling. If the building’s fume system groans or traffic inside the hood gets crowded, I speak up. Poor airflow means more risk. Careless or rushed work often brings accidents, so I keep only the bottles and tools I truly need out of storage.

Storage and Labeling Save Lives

Chemicals like 4-Bromo-2-Chlorofluorobenzene find their home in tightly closed containers, stashed in cool, well-ventilated spots. No direct sunlight. Sturdy shelves and clear labels matter. If a label falls off, I stop and solve the mystery—guesswork ruins safety. Any spill gets addressed right away, not at the end of the day.

I read the SDS (Safety Data Sheet) beforehand—the section on accidental release and exposure limits is crucial. Mixing this compound up with acids or strong oxidizers can get you into big trouble in a hurry.

Real-Life Practice Over Textbook Rules

Having emergency showers and eyewash stations set up nearby really does make a difference. Spills and splashes happen in seconds. I see many rely on “careful handling” as a catch-all solution, but being prepared to act on a spill beats trusting good luck. Labs should practice those drills regularly—knowing how to react keeps panic in check.

Accidents drop off fast when the people around me pay attention and talk about near misses. If someone slips up and gets a little too close to the fumes, the whole room should know. Lessons come from sharing. I try to foster that. Chemicals don’t care if someone’s new or has ten years in—they’ll treat us all the same.

Why Cutting Corners Isn’t Worth It

Safety means more than ticking boxes. Every shortcut gives danger a head start. From what I’ve seen, the safest labs work as a team. Everyone reminds each other about the basics. Respect for chemicals like 4-Bromo-2-Chlorofluorobenzene comes from sharing those daily experiences—what worked, what nearly failed, and what left a mark.

If you’re not sure how to handle this kind of compound, ask. A question now is easier than dealing with a burn or trip to the ER later. Staying curious and looking out for each other keeps everyone a little safer.

What is the purity specification for the available 4-Bromo-2-Chlorofluorobenzene product?

Understanding Purity: The Real-World Value

In chemical manufacturing, purity shapes everything from safety to performance. With 4-Bromo-2-Chlorofluorobenzene, the stated purity usually lands above 97%, and more than a few suppliers claim to hit 99%. Once in a while, material even tops 99.5%. This level of purity might look like a detail, but anyone working in synthesis or R&D knows why it keeps getting attention. At high purity, chemical reactions behave more predictably. Unexpected byproducts or process failures often trace back to impurities, not just technique. Anyone who has tried to troubleshoot contaminated batches understands the headaches involved.

The Importance Behind the Number

In the lab, high-purity material gives sharper results without unwanted side reactions. Low-level contaminants can sink a reaction yield or muddy up chromatography steps. Even in applications where "trace levels" seem fine, enough rounds of impurity exposure build up cross-contamination, especially when scaling up to kilo-quantities. Academic teams and pharmaceutical companies alike keep returning to high-purity standards for this reason. For medicinal chemistry, regulatory oversight puts even more weight on clean starting materials. It’s more than ticking a box: patient safety starts right at milligram scale.

Practical Insights on Specifications

Most reputable suppliers present a certificate showing the compound’s purity. Typical analytical methods include GC-MS, HPLC, and NMR, each with pros and cons for detecting different impurity types. I’ve compared reports myself—sometimes you spot a supplier using HPLC only, missing volatile contaminants that show up in GC-MS. That kind of detail matters if you work in sensitive synthesis environments.

Looking at common requirements, specifications such as “≥98%” or “≥99%” reflect what most synthetic chemists expect. From personal experience, anything under 97% purity creates frustration. Analytical departments spend time cleaning up missed impurities, interpret results with more caution, and ultimately, burn budget troubleshooting problems that didn’t have to crop up. Several chemists I know keep side-by-side samples from different suppliers and vet the in-house analysis just to confirm the numbers advertised. It’s almost a minor ritual before a big campaign.

Quality Control: Checking the Facts

Beyond supplier claims, it comes down to transparency. Trustworthy vendors show their lot-specific data and update their documentation regularly. A strong quality track record usually brings up better customer support, faster answers, and fewer surprises. A red flag pops up fast if a supplier dodges purity documentation or offers vague summaries. Labs can audit samples with independent testing, though lab time and budgets rarely stretch that far unless there’s a batch recall or inconsistent behavior in downstream chemistry.

Organizing Better Solutions

Pushing for more consistent quality is an industry-wide challenge. Large buyers can set specific purity criteria in their contracts, spelling out not just the number but also analytical methods and acceptance limits for known impurities. Small buyers can support their decisions by connecting with supplier technical staff and learning about the company’s quality processes, not just relying on a website checkbox. In some cases, buying a smaller sample lot for review before committing to bulk saves time and hassle over the long run.

At the end of the day, purity is far more than a number printed on a label. For those who work with 4-Bromo-2-Chlorofluorobenzene, that number stands between smooth progress and preventable setbacks. Quality, transparency, and smart quality control really decide the value you get.

4-Bromo-2-Chlorofluorobenzene
4-Bromo-2-Chlorofluorobenzene
Names
Preferred IUPAC name 1-Bromo-5-chloro-3-fluorobenzene
Other names 1-Bromo-3-chloro-4-fluorobenzene
4-Bromo-2-chloro-1-fluorobenzene
Pronunciation /ˈfɔːr ˈbroʊmoʊ tuː ˈklɔːroʊ ˈflʊəroʊ ˈbɛnziːn/
Identifiers
CAS Number 151059-47-5
3D model (JSmol) `/model/3d/JSmol.cgi?modelid=Mol-0001118079`
Beilstein Reference 795873
ChEBI CHEBI:132537
ChEMBL CHEMBL3722755
ChemSpider 20589564
DrugBank DB14683
ECHA InfoCard 03b3d1d8-2d68-423e-9f9b-0bace3aa9f9d
EC Number 636-695-1
Gmelin Reference 120047
KEGG C18438
MeSH D021483
PubChem CID 11794126
RTECS number CY8925000
UNII 07RA9A42J9
UN number UN3261
Properties
Chemical formula C6H3BrClF
Molar mass 207.44 g/mol
Appearance Colorless liquid
Odor Odorless
Density 1.73 g/mL at 25 °C (lit.)
Solubility in water Insoluble
log P 3.9
Vapor pressure 0.9 mmHg (20°C)
Acidity (pKa) pKa ≈ 43 (for the most acidic proton, typical of benzene derivatives)
Magnetic susceptibility (χ) NA
Refractive index (nD) 1.558
Viscosity 1.41 mPa·s (20 °C)
Dipole moment 2.61 D
Thermochemistry
Std molar entropy (S⦵298) 312.7 J·mol⁻¹·K⁻¹
Std enthalpy of formation (ΔfH⦵298) −48.0 kJ·mol⁻¹
Std enthalpy of combustion (ΔcH⦵298) -3685.8 kJ/mol
Hazards
GHS labelling GHS02, GHS07
Pictograms GHS07
Signal word Warning
Hazard statements H302, H315, H319, H335
Precautionary statements Precautionary statements: P261, P305+P351+P338, P337+P313
NFPA 704 (fire diamond) 2-2-0
Flash point 'Flash point: 86 °C'
Lethal dose or concentration LD50 Oral Rat 2914 mg/kg
LD50 (median dose) LD50 (median dose): Oral, rat: >2000 mg/kg
NIOSH BZ6300000
PEL (Permissible) Not established
REL (Recommended) Not established
Related compounds
Related compounds Bromofluorobenzenes
Chlorofluorobenzenes
Bromochlorobenzenes
2-Bromo-4-Chlorofluorobenzene
4-Bromo-2-fluoroaniline
4-Bromo-2-chlorophenol