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4-Bromobenzoxazole

    • Product Name 4-Bromobenzoxazole
    • Alias 4-Bromo-1,3-benzoxazole
    • Einecs 629-013-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
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    Specifications

    HS Code

    988302

    Product Name 4-Bromobenzoxazole
    Cas Number 23870-88-6
    Molecular Formula C7H4BrNO
    Molecular Weight 198.02 g/mol
    Iupac Name 4-bromo-1,3-benzoxazole
    Appearance Off-white to light brown solid
    Melting Point 151-154 °C
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles Brc1ccc2ocnc2c1
    Inchi InChI=1S/C7H4BrNO/c8-5-1-2-6-7(3-5)10-4-9-6
    Storage Temperature Store at 2-8°C
    Hazard Statements May cause irritation to skin, eyes, and respiratory tract

    As an accredited 4-Bromobenzoxazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of 4-Bromobenzoxazole

    Applications of 4-Bromobenzoxazole in Industrial Manufacturing

    As an experienced manufacturer, we supply 4-Bromobenzoxazole for technologically advanced, regulatory-driven sectors. Its molecular structure enables precise functionalization steps in target molecule synthesis. Below, you will find its validated roles in real, high-value downstream operations, with practical workflow details for active B2B customers.

    1. Pharmaceutical Intermediate for API Synthesis

    Many pharmaceutical producers use 4-Bromobenzoxazole as a core intermediate in the synthesis of advanced heterocyclic active pharmaceutical ingredients, especially within antibacterial and anticancer drug pipelines. Its bromine-substituted benzoxazole moiety is necessary for Suzuki or Buchwald–Hartwig coupling reactions, allowing medicinal chemists to introduce specific aromatic groups during lead candidate development, enabling precise API molecular design while maintaining route efficiency.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR 210/211: US cGMP regulations for drug substance production
    • Chinese Pharmacopoeia (ChP) requirements for chemical intermediates
    • EMA Guidelines for Genotoxic Impurities (for final API purity)

    Typical usage ratio

    • 5–20 mol% relative to target batch scale, tuned according to yield, throughput, and process safety studies

    Downstream process integration

    • Charging into palladium-catalyzed cross-coupling reactors for C–C or C–N bond formation
    • Integrated with inline HPLC monitoring for process QC
    • Used in multi-step organic syntheses under anhydrous, controlled temperature conditions

    Final product types

    • 3-substituted benzoxazole API intermediates
    • Novel antibiotics and kinase inhibitors
    • Route-specific oncology project substances
    • NDA-submitted final bulk APIs with benzoxazole scaffold

    2. OLED Material Precursor for Electronic Chemicals

    Specialty electronics makers utilize this compound as an integral aromatic building block in the synthesis of electron-transporting layers and functional emitters for organic light-emitting diode (OLED) displays and lighting. Its controlled reactivity and electron-rich backbone facilitate selective mono-substitution reactions, contributing to tailored optoelectronic performance and device lifetime. Process engineers value its high purity and reaction specificity for high-yield molecular design in emissive and transport layers.

    Industry compliance standards

    • IEC 60068: Electronic device chemical compatibility
    • RoHS 2011/65/EU Annex II compliance for restricted substances
    • JIS C62682: Organic electronics materials quality
    • In-house QC protocols for display-grade chemicals (trace metal, impurity profile)

    Typical usage ratio

    • 1–8 wt% in pre-polymer or precursor blends, optimized for film morphology and electrical performance

    Downstream process integration

    • Introduced in early synthetic steps for emitter and transporter molecules via halogen–metal exchange or direct coupling
    • Subjected to vacuum purification prior to device fabrication
    • Used in solution processing or vapor-phase deposition for thin-film production

    Final product types

    • Blue-green and deep-blue OLED emitting materials
    • Electron transport layer molecules
    • Small-molecule organic semiconductors
    • OLED display panel functional films

    3. Agrochemical Synthesis for Crop Protection

    4-Bromobenzoxazole functions as a selective intermediate for synthesizing heterocyclic herbicides and fungicides, particularly where benzoxazole linkage imparts metabolic stability and requisite soil activity. Agrochemical companies carry out condensation and further alkylation reactions on this scaffold, leveraging the reactivity of its bromine substituent for controlled ring functionalization. Precision control over impurity content is maintained to meet environmental and agricultural residue standards.

    Industry compliance standards

    • FAO/WHO specifications for pesticide technical material
    • REACH Registration (EC No. 1907/2006) for downstream use in EU
    • GB 2763: Maximum Residue Limits for Pesticides in Food (China)
    • ISO 9001:2015 quality management for agrochemical synthesis

    Typical usage ratio

    • 3–15 mol% in the formation of key fungicidal actives, modified based on complexity of the side-chain introduction and downstream transformation efficiency

    Downstream process integration

    • Used as initial step in N-alkylation or Suzuki–Miyaura coupling for active ingredient frameworks
    • Batch-wise addition under inert gas in multi-stage synthesis
    • Subjected to chromatographic purification for high-grade actives

    Final product types

    • Benzoxazole-based herbicide intermediates
    • Broad-spectrum cereal fungicides
    • Rice and wheat crop protection actives
    • Technical grade agrochemical concentrates

    4. Specialty Dye Manufacturing for Polymer Fibers

    Some specialty dye companies incorporate this molecule to synthesize benzoxazole-containing dyestuffs, introducing chromophores with high bathochromic shifts for advanced textile and technical fiber coloration. The compound enters key steps where controlled bromination ensures fidelious color tuning and fastness properties in acid, disperse, or reactive dye types. Experts design recipes balancing reactivity for optimal color development and compatibility with polyester or aramid polymer chains.

    Industry compliance standards

    • OEKO-TEX Standard 100 (test for residuals in textile dyes)
    • EN 71-3: Chemical safety in colored articles
    • GOTS (Global Organic Textile Standard) restricted substances list
    • ZDHC MRSL: Manufacturing Restricted Substances List (dye process)

    Typical usage ratio

    • 2–12 mol% depending on dye chromophore type and fiber substrate, adjusted for shade strength and fixation percentage

    Downstream process integration

    • Engaged in diazo coupling or condensation with chromophoric auxiliaries for colorant synthesis
    • Included at early step for aramid dye pre-intermediates
    • Purification via silica gel or column chromatography prior to blending with dispersants

    Final product types

    • High-performance polymer-compatible dye intermediates
    • Reactive and acid dyes for technical textiles
    • Colorants for polyester and high-tenacity fibers
    • Functionalized textile dye blends for export

    5. Analytical Standard for Environmental Monitoring

    Environmental labs and analytical firms require benzoxazole derivatives as spiking and reference standards for monitoring contamination in water and soil. The monobromo derivative’s purity and unique chromatographic behavior make it suitable for calibrating HPLC and GC-MS systems. Accurate quantification studies of agrochemical residues or emerging contaminants often rely on such specialty chemicals for robust method validation and regulatory reporting.

    Industry compliance standards

    • ISO/IEC 17025: Laboratory competence (testing and calibration)
    • EPA Methods 8081/8321 for semi-volatile organics (US)
    • EN 16693: Analytical standards performance
    • Good Laboratory Practice (GLP) principles (OECD #1)

    Typical usage ratio

    • 1–100 µg/mL as calibration or control standard, with adjustments based on matrix and detection limit requirements

    Downstream process integration

    • Dissolved in HPLC/GC-grade solvents for calibration solution preparation
    • Added to matrix samples or surrogates at method development stage
    • Applied in recovery studies and validation protocols during sample testing

    Final product types

    • Certified reference calibration solutions for analytical use
    • Custom analytical standards for environmental monitoring panels
    • Proficiency testing kits for laboratory QC
    • Internal standards for trace residue analysis
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    More Introduction

    4-Bromobenzoxazole: A Closer Look at Its Role and Relevance

    Science marches forward on the back of specialized building blocks—some better known than others. 4-Bromobenzoxazole marks its territory as one of those less flashy, yet remarkably useful compounds. Its place spans from research labs to advanced manufacturing settings, carrying an impact that radiates beyond its minimal media coverage. In my years working alongside chemists and engineers, I’ve often witnessed how the smallest tweaks to molecules shape the progress of entire industries. 4-Bromobenzoxazole lends itself well to this role, and it rarely gets the discussion it deserves.

    Understanding the Basics

    4-Bromobenzoxazole stands as a brominated derivative of benzoxazole, characterized by the presence of a bromine atom attached to the fourth position of the benzoxazole ring. This subtle alteration brings new chemical reactivity while keeping the compact, rigid structure that defines benzoxazoles. Chemically, it appears as a crystalline solid—something you’d gloss past in a lab notebook unless you’re the sort who likes to dig into why that extra bromine matters.

    This compound finds its home in a crowded family of heterocycles, molecules where one or more atoms in the ring are not carbon—here, we get nitrogen and oxygen. The benzoxazole ring itself is no stranger to many fields, valued for its electron-rich structure and remarkable stability. Drop a bromine onto it, and the possibilities shift. You notice big changes in reactivity, solubility, and safety profile, each of which affects how chemists approach real-world challenges.

    Model and Key Specifications

    I remember the first time someone handed me a sample: a fine, almost chalky powder in a glass vial. 4-Bromobenzoxazole typically shows up as an off-white to yellowish solid. Its molecular formula, C7H4BrNO, packs a decent punch, with a molecular weight pushing just past 198 g/mol. Purity levels matter—often, researchers want more than 98%—and suppliers keep a close eye on trace impurities, moisture content, and storage conditions. Even a bit of degradation can mean the difference between a reaction that runs smoothly and one that fails without warning. Those who spend any time working with high-precision organic reactions know the pain that comes from overlooked contaminants.

    The structure itself is telling. The fused benzene and oxazole rings share electrons, creating a stable base. The bromine hangs off the fourth carbon, about as far from the nitrogen as you can get in such a tight ring. This position affects not just the look but the way reagents approach the molecule in a flask.

    Where 4-Bromobenzoxazole Makes Its Mark

    Practicality drives adoption. 4-Bromobenzoxazole lands at the crossroads of synthetic organic chemistry, materials science, and even pharmaceuticals. Over my career, the compound has cropped up in several places: as a precursor in the creation of novel heterocyclic targets, an intermediate in drug manufacture, and a participant in functional material development. For chemists hunting fresh scaffolds for biologically active molecules, brominated benzoxazoles offer an easy point of modification. The bromine at position four opens up the door for substitution reactions, especially palladium-catalyzed cross-couplings like Suzuki or Buchwald-Hartwig aminations. Anyone who’s pushed the boundaries of synthesis knows the frustration of not having the right functional handles. Here, the bromine acts as a reliable entry point for further modification.

    I’ve spoken with researchers who rely on 4-bromobenzoxazole for stepwise construction of fluorescent probes, agrochemical candidates, and even polymer precursors. In the pharmaceutical world, compact heterocyclic cores serve as essential skeletons—starting from 4-bromobenzoxazole simplifies the construction of derivatives with anti-inflammatory, antimicrobial, or anticancer properties. Nature does a lot with small tweaks to chemical frameworks, and chemists mimic that efficiency by starting with smart building blocks.

    Why Does the Bromine Matter?

    It’s easy to overlook the strength of a single atom change. Bromine brings both heft and reactivity. Placed at this strategic position, it alters electron distribution and chemical behavior in measurable ways. In reactions, this bromine acts not just as a passive spectator but as a gatekeeper. Its presence makes the molecule more amenable to halogen-metal exchange, allowing for rapid transformation into a host of new compounds.

    You can see the impact especially in cross-coupling chemistry. Coupling reactions demand a good leaving group—bromine fills this role nicely, and its position on the benzoxazole ring speeds up reactions that otherwise crawl along. This efficiency cuts costs and headaches in scale-up, a fact more important than ever as researchers work to minimize both environmental burden and financial risk.

    Comparisons with Other Benzoxazoles and Brominated Compounds

    Stepping back, several benzoxazole derivatives crowd the market, but few line up head-to-head with 4-bromobenzoxazole across all metrics. Take the unsubstituted benzoxazole: stable, useful, but not nearly as reactive. The addition of a bromine not only increases molecular weight but enhances functionality for downstream applications. Other bromobenzoxazoles, such as those with bromine hanging off the second or sixth position, end up with different reactivity and face selectivity issues that make chemistry less predictable.

    Against the wider universe of halogenated aromatics, bromine brings a mildness compared to iodine but leaves more of an impact than chlorine. Iodine might offer even higher reactivity in some coupling reactions, but it often comes with higher costs and greater toxicity. Chlorinated analogues, though cheaper, tend to underperform in the same cross-couplings or require harsher conditions. Chemists, myself included, gravitate toward brominated intermediates as a reasonable compromise between cost, utility, and safety.

    Working Conditions and Handling

    Anyone dealing with aromatic chemicals knows the importance of good handling practices. 4-Bromobenzoxazole, like most small-molecule benzoxazoles, doesn’t carry substantial acute toxicity in small quantities. Still, it pays to respect all organic reagents: gloves, goggles, and well-ventilated hoods prove their worth over the years. Even low-toxicity materials demand mindfulness, since chronic exposure can build up problems not visible after a single day’s work. I once witnessed a minor mishap where a careless approach to dust control led to contamination—the time and resources lost in the cleanup far exceeded what anyone expected.

    As with most organic solids, storing 4-bromobenzoxazole in tightly sealed, light-resistant containers keeps it at its best. Prolonged exposure to air or moisture risks slow decomposition. While not as sensitive as some peroxides or alkali metals, it rewards care.

    Usage in Research and Industrial Contexts

    In the research world, speed and flexibility rule. 4-Bromobenzoxazole fits into synthetic strategies for constructing libraries of new molecules. Those studying medicinal chemistry appreciate its versatility, using it to build up complex molecular frameworks required for testing new drug candidates. I’ve seen projects accelerate when the right functional handle, like the bromine here, unlocks entire classes of derivatives previously out of reach. As someone who’s spent hours patching together multi-step syntheses, the time saved is significant.

    Industrial applications take this a step further. Bulk manufacturing leans on intermediates that react efficiently and predictably. Process engineers face a mess of challenges—yield, waste management, reproducibility, and cost. The reliability of cross-coupling reactions off the bromo group translates into smoother scale-up and fewer surprises at production scale. This level of predictability in batch processes can mean the difference between a promising project and one that never leaves the lab.

    Practical Challenges and Solutions

    One challenge always comes up: availability and consistency of supply. Specialty chemicals such as 4-bromobenzoxazole can disappear from catalogs due to raw material shortages or shifts in supplier priorities. Over the years, I’ve learned that building solid relationships with reputable suppliers curtails unexpected shortages. Buying in bulk and maintaining a buffer stock ensures that essential research or manufacturing schedules don’t grind to a halt. When price spikes or purity batches swing, groups with long-term supplier partnerships fare better, adjusting to disruptions with less pain.

    Another headache relates to scale. Lab synthesis often runs on a few grams, but scale-up introduces new issues: managing heat, ensuring even mixing, and dealing with more waste. Small variations in reagents or solvent quality, overlooked at bench scale, turn into safety or yield headaches on the kilo scale. Firms investing in robust process development early find fewer surprises later. Standardizing procedures, frequent pilot runs, and incorporating automation all whittle down the risks.

    Waste disposal can’t be brushed aside. Halogenated organic waste piles up quickly in any setting using 4-bromobenzoxazole as an intermediate. Strict protocols for chemical waste, investment in on-site neutralization, and clear policies for hazardous material handling speak to a responsible research environment. With increasing global scrutiny and evolving regulations, the companies and labs who do this best are already ahead of the curve.

    Future Perspectives: 4-Bromobenzoxazole’s Evolving Role

    Chemical research and manufacturing don’t sit still, and neither do the demands for improved intermediates. Researchers continue to find inventive uses for 4-bromobenzoxazole: late-stage functionalization of complex molecules, preparation of materials with specialized luminescent or electrical properties, and development of new catalysts. In conversations with material scientists, I’ve gathered that the molecule’s rigidity and electron-rich core play a role in the development of new polymeric materials for electronics and optics. Sometimes the right starting point is all it takes to unlock innovation.

    Green chemistry remains a growing concern. Several academic groups and startups are working to improve the environmental impact of halogenated heterocycles. That might mean more efficient synthetic routes, better recycling of halide byproducts, or development of greener cross-coupling protocols. I’ve sat in meetings where the choice of solvent or reagent gets as much discussion as the chemistry itself—a sign that those in the field are looking after more than just immediate results.

    Cultivating Expertise and Sharing Knowledge

    It’s not just about access to chemicals but the way we talk about and share their value. 4-Bromobenzoxazole may be a small player on the big stage, but giving it attention opens new discussions. Its clear niche, combined with a manageable risk profile and flexibility, makes it an object lesson in the importance of thoughtful intermediate selection. As those who’ve had hands-on experience know, success in research and industry often comes from the intersection of small details and broad understanding.

    Mentoring younger chemists, I’ve found it useful to point to real-world applications—such as how one atom shift can change the outcome of an entire project. Rolling these insights into practical guidance helps others avoid common pitfalls, whether in scaling up new processes or designing greener experiments. Sharing stories, close calls, and unexpected wins builds a collective wisdom that benefits both the individual researcher and the broader community.

    Integration with Digital and Predictive Tools

    Chemistry labs look different today than they did a decade ago. Computational models help predict how 4-bromobenzoxazole and related compounds will perform across reactions. Data analysis tools, increasingly powered by machine learning, recommend conditions that maximize yield or cut waste. I’ve worked on projects where running simulations around this single intermediate saved weeks of experimental work. The combination of hands-on expertise and digital support means fewer blind alleys.

    Digitalization also aids in tracking supply chains and managing compliance with new safety and environmental standards. Modern inventory systems alert labs when stocks fall too low or shelf lives expire, reducing both financial loss and risk. Research institutions that invest in these tools find themselves with more time for creative work, since they spend less time firefighting unexpected equipment and supply failures.

    Community Building and Standards

    No chemical operates in isolation; real progress comes out of collaboration across backgrounds. Consistent standards for handling, purity, and documentation help ensure that 4-bromobenzoxazole findings can be reproduced anywhere. Chemists who embrace community-driven best practices make their work more useful to others. Publishing clear synthetic procedures, thorough analytical data, and honest accounts of setbacks—as well as successes—contributes to a more resilient discipline. The broader acceptance of open-access publishing and preprints builds momentum here, and it’s gratifying to see more young researchers joining the effort.

    Conclusion: The Unsung Value of Specialized Intermediates

    With so much focus on breakthroughs and end products, it’s easy to overlook the workhorses that underpin progress. 4-Bromobenzoxazole sits squarely in that category. Chemists, material scientists, and engineers value it because it performs where it counts—facilitating reactions, building up complexity, and saving time and resources in both early development and mature processes. Its sensible risk profile and relative ease of use ensure it will keep a foothold in labs for years to come.

    The story of 4-bromobenzoxazole isn’t just about atoms and bonds. It’s about the thoughtful choices made by those who shape technology, health, and our understanding of the world, one reaction at a time. In my experience, paying attention to these details—while staying connected with colleagues and open to new ideas—keeps the field both productive and grounded for the future.