|
HS Code |
285669 |
| Productname | 2-Bromo-4-Fluoro-6-Methylbenzonitrile |
| Casnumber | 127654-02-2 |
| Molecularformula | C8H4BrFN |
| Molecularweight | 214.03 |
| Appearance | White to off-white solid |
| Meltingpoint | 56-60°C |
| Boilingpoint | 276°C at 760 mmHg |
| Density | 1.61 g/cm3 |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | CC1=C(C=CC(=C1Br)F)C#N |
| Inchi | InChI=1S/C8H4BrFN/c1-5-6(4-11)2-3-7(10)8(5)9 |
| Synonyms | 2-Bromo-4-fluoro-6-methylbenzenecarbonitrile |
| Storagetemperature | Store at 2-8°C |
As an accredited 2-Bromo-4-Fluoro-6-Methylbenzonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | |
| Shipping | |
| Storage |
Competitive 2-Bromo-4-Fluoro-6-Methylbenzonitrile prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
Specialty chemicals play a bigger role in our lives than most people notice. Inside every new material or lifesaving drug, organic chemists rely on reliable starting points to build complex molecules. 2-Bromo-4-Fluoro-6-Methylbenzonitrile stands out as one of those underappreciated workhorses. Its chemical formula—C8H5BrFN—comes with a unique mix of halogen atoms that unlock possibilities across research, manufacturing, and applied chemistry. Most labs and pilot plants seeking aromatic nitriles with precision placement of methyl, fluoro, and bromo groups find this compound indispensable.
The fundamental structure of this compound brings together a trifecta of substitutions on the benzene ring: a bromine at the 2-position, a fluorine at the 4-position, and a methyl group at the 6-position. There’s also a nitrile group that adds synthetic utility. This pattern of substitution can make a world of difference when designing new pharmaceuticals or agricultural chemicals. As each position on the ring interacts differently with neighboring groups, this precise arrangement delivers selectivity chemists can count on. For example, the presence of a bromine offers an effective entry point for further transformations using palladium-catalyzed cross-coupling reactions. Both the fluoro and methyl substituents adjust the electron density, driving directed synthesis in ways that plain benzonitriles simply can’t match. From my own experience in an academic lab, similar compounds proved essential for stimulating otherwise sluggish transformations, thanks to such well-placed halogens.
This aromatic nitrile appears as a pale solid under standard conditions and usually arrives in airtight containers that protect from moisture and light. The product generally boasts a purity upwards of 98 percent when sourced from reputable suppliers, ensuring that downstream reactions remain consistent and reproducible. The melting point typically falls within a narrow range suitable for storage and direct use in most lab environments. Many professionals find it straightforward to handle using gloves and standard safety practices, as the nitrile group also keeps volatility within reasonable bounds. Unlike some multi-halogenated aromatics, the presence of the methyl and fluoro groups reduces the propensity for rapid degradation, both in storage and during reactions.
The true strength of 2-Bromo-4-Fluoro-6-Methylbenzonitrile shows up in its flexibility as a synthetic intermediate. The pharmaceutical industry relies heavily on aromatic nitriles for their role in active pharmaceutical ingredient (API) development. The unique substitution pattern allows medicinal chemists to test new scaffolds, especially when searching for improved bioavailability or target selectivity. Agrochemical researchers use nitrile compounds with halogen and methyl groups to design crop protectants that keep pests at bay without causing excess toxicity to plants. Material scientists also pay attention, since the electronic properties of this substituted ring system can influence conductivity and thermal stability in advanced polymer applications.
From a practical angle, this intermediate lets researchers move from proof-of-concept reactions in a small vial to scalable syntheses at the pilot plant. Whether the aim is to build out aniline derivatives, forge new bonds using classic Suzuki or Buchwald-Hartwig reactions, or manipulate the nitrile for carboxylic acid synthesis, this compound delivers a solid head start. In my work with heterocyclic scaffolds, having a methyl group that stands up to a broad range of conditions proved invaluable. The methyl at the 6-position doesn’t just serve as a placeholder—it influences regioselectivity in every significant downstream reaction.
Plenty of aromatic nitrile building blocks exist. What sets this compound apart is the specific arrangement of the substituents. Compare it to 2-Bromo-4-Fluorobenzonitrile: you miss out on the steric and electronic effects offered by that extra methyl group. Without methyl, some reactions run slower or lead to messy byproducts due to uncontrolled orientation during functionalization. Engineers designing new sensors or optical materials see measurable changes in response when switching between single- and multi-substituted benzonitriles.
Even more stark differences surface if one leaves out the bromo or fluoro positions. Lab colleagues would vouch that the bromo group, for example, acts like a Swiss Army knife in cross-coupling chemistry. Drop it from the molecule and the utility drops off sharply. Meanwhile, fluorine subtly tunes reactivity and biological compatibility. In robust pharmaceutical workflows, the right substitution pattern can shave weeks off a synthesis campaign, saving resources and keeping projects on track. Switching to compounds with less strategic substitution usually forces more steps and lower yields. That’s experience I would rather avoid.
Supply chain reliability means more than just having inventory on a shelf. Chemists want to avoid surprises that could throw off entire research timelines. During periods of increased demand—such as a broad push towards new antiviral drugs—access to specialty building blocks like this one determines whether projects advance or languish. The global shift toward greener production methods has also raised the bar on transparency. Both academic and industrial chemists expect clear documentation on source quality. Suppliers who provide up-to-date certificates of analysis help boost trust, particularly among regulatory-conscious pharmaceutical teams.
At a time when R&D budgets are closely watched, a dependable source cuts the risk of lost batches or repeat syntheses. Researchers lose patience quickly if batches of an intermediate arrive with variable purity, off-putting odors, or unanticipated water content. Factoring in the true cost of rework, most modern organizations opt for certified suppliers, even at a slight premium. Reliable supply extends well beyond the first delivery; it tracks closely with the ability to fulfill long-term framework agreements and to respond rapidly if custom batch sizes are needed.
Every specialty chemical carries safety and environmental considerations. 2-Bromo-4-Fluoro-6-Methylbenzonitrile stands as a safer alternative to many polyhalogenated aromatics, which often present a higher risk of environmental persistence. Industry observations suggest its toxicity profile falls within the expected range for single-digit millimolar aromatic nitriles. Still, conscientious chemists don proper personal protective equipment, including gloves and goggles, to avoid unintentional contact. Good ventilation and proper waste collection also go hand-in-hand with responsible laboratory use. This product usually avoids the worst reputational baggage because it doesn’t generate ozone-depleting waste or degrade into highly persistent pollutants.
Waste management systems equipped to deal with halogenated organics handle benzonitrile derivatives routinely. As someone who spent many past nights double-checking waste codes, I appreciate intermediates with a clear path for compliant disposal. Regulatory agencies continue pushing tighter scrutiny around solvents and byproducts, placing even more value on compounds where environmental documentation comes standard. Rising awareness of green chemistry motivates ongoing improvements in both synthesis and downstream management.
Most people devote little thought to the raw materials behind medicine or new batteries, but that invisible network does the heavy lifting. My experience in bench chemistry taught me that the quality of basic building blocks sets the tone for months of research. A single batch of poorly characterized aromatic intermediate caused cascading setbacks, teaching all involved the value of traceability in procurement. The right intermediate, sourced with consistent purity, often turns out to be the thread connecting innovation to application. Colleagues working in drug discovery share similar tales—sometimes success comes down to a handful of grams of a single well-made compound.
Direct engagement with reputable suppliers brings another layer of assurance. People who answer detailed technical questions, and who understand the end uses of each batch, help keep projects on solid footing. More suppliers today invest in training local staff and maintain open lines for transparency. The industry takes pride in these relationships, seeking long-term partners rather than faceless transactions. This culture shift benefits everyone trying to move bold ideas from the whiteboard to a tangible product.
Today’s market increasingly demands more than just a chemical with a clean label. Pharmaceutical regulators want documented traceability, clear evidence of compliance with REACH or other relevant frameworks, and full transparency in the supply chain. Supplier audits are no longer rare events—they come with real follow-up and sometimes, third-party verification. As a practitioner who has weathered several rounds of regulatory scrutiny, I can confirm that robust paperwork often matters as much as product purity.
This compound, with its well-defined structure and manageable hazard profile, regularly meets the hurdles set by regulators—provided suppliers keep up their end. Testing protocols must confirm not just composition but also the absence of unwanted side-products or residual solvents. Modern analytical equipment like HPLC and NMR ensure that every lot meets stringent performance criteria. Researchers who draw on these assurances work with more confidence, even under tight delivery schedules or evolving compliance regimes.
Scientific progress builds on reliable starting points. While it might feel tempting to brush off stepwise intermediates as mere commodities, each one tells a story about attention to detail and trust in supply networks. In my own lab, we encountered bottlenecks whenever supply chains wavered—lost time, repeated syntheses, and tight budgets stretched thin. Every delay ripples through the grant cycle and stresses collaborative relationships across institutions.
Solving these problems depends on more than logistics. Cross-talk between synthesis teams, procurement officers, and regulatory experts ensures that essential intermediates like 2-Bromo-4-Fluoro-6-Methylbenzonitrile keep flowing. Open feedback between scientists and suppliers creates room to flag formulation improvements or faster lead times. The industry trend points toward closer partnerships, with scientists at the bench contributing to supplier quality systems and vendors reciprocating with technical advice. Keeping these channels open remains the surest path to overcoming bottlenecks and pushing scientific boundaries.
Every intermediate with unique substitution patterns drives innovation somewhere downstream. The subtle tweaks that chemists introduce—such as precisely placing a methyl group or selecting a particular halogen—cause dramatic shifts in biological response or material characteristics. Experienced professionals learn quickly to value these properties when patents or publications are at stake. I remember projects where a single small change to an intermediate opened a path to entirely new molecular families. Those moments underscore the real-world impact of getting a reliable, well-characterized supply.
The pharmaceutical pipeline draws heavily on intermediates that allow for rapid analog synthesis. When each new molecule costs thousands in reagents and weeks of time, the flexibility offered by compounds like this one pays off handsomely. The trend toward personalized medicine and increasingly targeted therapies only raises the stakes. Material science, too, leans on fine-tuned intermediates that turn research-grade polymers into high-performance films, fibers, or coatings. This downstream agility all starts with stable sources of specialty molecules.
No industry stands still, and specialty chemicals are no exception. Efficiency in manufacturing, better green chemistry integration, and wider access to certified material have all come to the fore. Researchers and suppliers alike are shifting toward greener synthetic pathways, sometimes swapping out traditional solvents for more sustainable options or improving yields to reduce waste. In my own experience, the growing availability of process data and feedback loops between customer and supplier speed up these improvements. Suppliers who respond quickly to technical queries or who design custom batches on short notice help keep R&D functioning at full speed.
New areas also open up every year. For instance, with rising interest in fluorinated pharmaceuticals—renowned for their metabolic stability—the demand for starting materials like this one increases. The expansion of chemical recycling technologies could soon allow more efficient capture and re-use of multi-substituted aromatics, easing both supply and waste burdens.
Educators and mentors in chemistry sometimes stress the importance of “thinking from the molecule up.” This philosophy rings true for anyone invested in applied science. By focusing on the practical building blocks and the people who produce them, the broader research community learns the value of clear communication and shared standards. In smaller-scale academic labs, partnerships with chemical suppliers often make the difference between a shelved project and a published paper.
As the industry moves toward more collaborative, transparent supply chains, everyone benefits. Students working with these intermediates gain exposure to real-world problems, from procurement challenges to regulatory hurdles. Professional societies and technical groups invest in best practices, supporting newcomers and veterans alike in navigating an increasingly complex industry.
Behind every novel drug, advanced circuit, or innovative polymer lies a chain of choices and partnerships that keep progress moving. 2-Bromo-4-Fluoro-6-Methylbenzonitrile, with its unique blend of halogen and methyl groups, serves as a reliable anchor in this process. For the chemists, engineers, and technical teams who work tirelessly from discovery to production, this intermediate stands as a testament to the rewards of detail, trust, and ongoing collaboration. As research tackles tougher challenges and the boundaries of possibility expand, dependable, well-characterized intermediates hold the key to what’s next.