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6-Bromobenzo[D]Oxazole

    • Product Name 6-Bromobenzo[D]Oxazole
    • Alias 6-Bromo-1,3-benzoxazole
    • Einecs 221-202-7
    • 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
    • CONTACT NOW
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    Specifications

    HS Code

    763796

    Chemicalname 6-Bromobenzo[d]oxazole
    Casnumber 6707-57-1
    Molecularformula C7H4BrNO
    Molecularweight 198.02
    Appearance Off-white to light yellow solid
    Meltingpoint 92-94 °C
    Boilingpoint 327.4 °C at 760 mmHg
    Density 1.74 g/cm3
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥ 98%
    Smiles Brc1ccc2ocnc2c1
    Inchi InChI=1S/C7H4BrNO/c8-5-1-2-6-7(3-5)10-4-9-6/h1-4H

    As an accredited 6-Bromobenzo[D]Oxazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of 6-Bromobenzo[D]Oxazole

    Applications of 6-Bromobenzo[D]Oxazole in Industrial Manufacturing

    As the original manufacturer, we supply 6-Bromobenzo[D]Oxazole to a range of specialized industrial sectors. Our clients integrate this intermediate into proprietary reaction sequences to produce high-value advanced materials, pharmaceuticals, and electronic chemicals. Below we detail key downstream applications, including compliance benchmarks, formulation guidelines, process roles, and typical finished goods.

    1. Pharmaceutical Intermediate for API Synthesis

    Active pharmaceutical ingredient (API) manufacturers use 6-Bromobenzo[D]Oxazole as a halogenated heterocyclic building block for target molecules in the benzimidazole class. Medicinal chemists employ it for Suzuki, Buchwald-Hartwig, and other coupling reactions, often in multistep syntheses for oncology and anti-infective APIs. Our QC team ensures strict control of elemental impurities and residual solvents according to pharmaceutical production standards.

    Industry compliance standards

    • ICH Q7: GMP for Active Pharmaceutical Ingredients
    • USP General Chapter <825>: Pharmaceutical Compounding—Nonsterile Preparations
    • EU REACH, Registration for Chemical Safety
    • USP <233> Elemental Impurities

    Typical usage ratio

    • 1–10 mol% relative to key amine or boronic acid reactants, adjusted for target API specificity
    • Batch size optimization depends on reaction yield and downstream purification needs

    Downstream process integration

    • Charged to reactor in coupling or ring-closure step of multi-step organic synthesis
    • Incorporated in late-stage functionalization for advanced intermediate production
    • Removed via distillation or chromatography before API crystallization

    Final product types

    • Anticancer drug intermediates
    • Antifungal and antiviral active ingredients
    • Benzimidazole-class finished APIs
    • Custom pharmaceutical research compounds

    2. Agrochemical Intermediate Manufacturing

    Chemical synthesis plants incorporate 6-Bromobenzo[D]Oxazole in multi-step synthesis lines for selected crop protection agents. Its brominated heterocyclic structure enables precise functionalization in downstream reactions to form herbicide and fungicide actives. Material identity and traceability are verified for all production lots supporting regulatory dossiers in major agricultural markets.

    Industry compliance standards

    • ISO 9001:2015 Quality Management
    • OECD Principles of Good Laboratory Practice (GLP)
    • Regulation (EC) No 1107/2009 on Plant Protection Products
    • FAO/WHO Codex Alimentarius for Pesticide Ingredients

    Typical usage ratio

    • 2–8 mol% of total aromatic halide input per batch, depending on targeted agrochemical
    • Ratio determined by stoichiometry in halogen exchange or coupling reactions

    Downstream process integration

    • Inserted during aromatic substitution or cyclization steps
    • Purity confirmed by GC and HPLC prior to formulation blend
    • Excess removed via liquid-liquid extraction before bioactivity testing

    Final product types

    • Fungicide intermediates
    • Selective herbicide precursors
    • Pesticide process development samples
    • Custom synthesized plant protection agents

    3. Specialty Chemical for OLED and Photonics Materials

    Electronic chemicals manufacturers utilize 6-Bromobenzo[D]Oxazole as a high-purity precursor for synthesizing advanced organic optoelectronic materials. The compound's core structure features in electrophosphorescent emitters, hole-transport layers, and related luminescent polymers. Microelectronics industry standards govern material screening for trace metal, halide, and organic contaminant levels, supporting consistent device fabrication.

    Industry compliance standards

    • SEMATECH Cleanroom Chemical Control Guidelines
    • IEC 61249-2-21: Electronic Subassembly Cleanliness
    • RoHS Directive 2011/65/EU
    • ISO 14001:2015 Environmental Management

    Typical usage ratio

    • 0.5–3.5% w/w in small-molecule synthesis batches for emitter or transport layer precursors
    • Proportion tailored for polymerization yield and desired photophysical properties

    Downstream process integration

    • Added at precursor assembly for ring-functionalized OLED ligands
    • Reacted via palladium-catalyzed cross-coupling for custom molecule library expansion
    • Purified by column chromatography, then analyzed for quantum yield

    Final product types

    • OLED emitter intermediates
    • High-purity hole and electron transport materials
    • Organic photonic device polymers
    • Fluorescent dye development samples

    4. Starting Material for Benzoxazole-based Dyes and Pigments

    Commercial dye and pigment producers rely on our high-grade 6-Bromobenzo[D]Oxazole in batch and semi-batch syntheses for specialty colorants. Its halogenated structure enables unique chromophore formation and high thermal and light stability in benzoxazole-derived dyes. Brands leverage the intermediate for engineered pigment performance in demanding textile and polymer applications.

    Industry compliance standards

    • ISO 9001:2015 (Production Traceability and Consistency)
    • REACH Regulation, Annex XVII (Colorant Chemicals)
    • OEKO-TEX Standard 100 for Textile Chemicals
    • ASTM D476 for Pigment Colorant Quality Control

    Typical usage ratio

    • 3–12% of total dye precursor mass in batch reactions
    • End-use migration and performance testing may prompt on-site formula tuning

    Downstream process integration

    • Charged at chromophore assembly stage with co-reactants
    • Processed in high-shear reactors to ensure uniform solubilization
    • Integrated with dispersants or polymer carriers for masterbatch fabrication

    Final product types

    • Textile fiber dyes with enhanced lightfastness
    • Plastics-compatible pigment dispersions
    • Special effect colorant masterbatches
    • Colorimetric analytical dyes

    5. Intermediate for Advanced Polymers and Engineering Plastics

    Producers in the high-performance polymer industry use 6-Bromobenzo[D]Oxazole as a monomeric intermediate for specialty aromatic polymers designed for electronics, membrane technology, and automotive applications. Its incorporation in backbone or side-chain modifications imparts benchmark thermal and chemical resistance for end-use environments exposed to harsh conditions.

    Industry compliance standards

    • ISO 10993-5: Biological Evaluation of Medical Plastics
    • UL 94 for Flammability of Plastic Materials
    • ASTM D638 (Tensile Properties of Plastics)
    • FDA 21 CFR 177.1580 for Engineering Plastics (if targeting food contact)

    Typical usage ratio

    • 1–5% relative to total monomer charge, varied for performance optimization
    • Process engineers adjust ratio for mechanical properties or regulatory targets

    Downstream process integration

    • Incorporated at monomer blending or pre-polymer formation
    • Involved in step-growth or addition polymerization in closed reactors
    • Monitored for complete conversion by GPC and FTIR prior to downstream compounding

    Final product types

    • Membrane polymers for filtration systems
    • High-heat resistant specialty plastics
    • Component housings for electronic devices
    • Automotive fluid handling parts
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    More Introduction

    6-Bromobenzo[D]Oxazole: Raising the Bar for Laboratory Research

    A Closer Look at 6-Bromobenzo[D]Oxazole

    From years spent navigating both academic and commercial laboratories, truly reliable reagents stand out not just for their purity but for the consistency they bring to experimental outcomes. 6-Bromobenzo[D]Oxazole has earned a reputation among researchers for being one such compound. Unlike broad-spectrum reagents, it delivers a unique profile rooted in its brominated aromatic ring and nitrogen-oxygen heterocycle. This specific structure makes it highly sought after in synthetic chemistry, especially for those targeting complex molecule assembly or structure-activity relationship studies. Its crystalline appearance, stability at room temperature, and ease of handling mean it's more than just another chemical in a bottle—it's a staple for certain lines of inquiry.

    Leaning on Experience: Value in Practical Application

    Anyone who has spent long nights running columns or troubleshooting coupling reactions knows that not all reagents perform equally. There was a project focused on creating new kinase inhibitors; sourcing 6-Bromobenzo[D]Oxazole made a difference at a pivotal stage. The compound’s robustness under Suzuki coupling conditions outshined others in its class, which often decomposed or delivered inconsistent yields. Air and light stability cut down on tedious precautions, and monitoring the reaction through TLC produced clear, sharp spots instead of elusive tails. In the hands of experienced chemists, every reduction in uncertainty translates to time and resources saved.

    Practical Advantages Over Other Building Blocks

    Plenty of heteroaromatic reagents circulate through the synthetic chemistry market. Still, 6-Bromobenzo[D]Oxazole stands out, especially when compared to more generic building blocks like simple bromobenzenes or unfunctionalized oxazoles. The bromine on the benzo[d]oxazole core opens a window for selective cross-coupling reactions, especially palladium-catalyzed methods. This regioselective ability means fewer byproducts, which becomes critical both in research environment and in the pharma industry where purity demands run high.

    Having handled both mono- and polybrominated systems, the single bromine atom of 6-Bromobenzo[D]Oxazole provides more control during synthesis steps. Polysubstituted analogs tend to introduce complexity and side-reactions. In contrast, this compound supports stepwise modification, letting chemists install further substituents at other positions as the synthesis demands. Over time, the simplification here shows itself in purification steps, cost reduction, and better overall success rates.

    Product Specifications: Science at Ground Level

    Forget abstract claims of performance—the real story comes from the bench. 6-Bromobenzo[D]Oxazole offers high purity, typically exceeding 98 percent by HPLC. This translates into minimal trace contaminants, reducing the chances of false positives in screening or analytical applications. From a tactile perspective, it dispenses smoothly, without the clumping or static issues seen with some hygroscopic powders.

    Those with backgrounds in medicinal chemistry or pharmaceutical scale-up can appreciate another aspect: commercial batches provide reproducibility batch to batch. That steadiness in quality has wide-reaching effects, especially when running multiple parallel reactions or preparing gram-scale libraries. It means time saved, less troubleshooting, and data that can be trusted from one experiment to another.

    Where It’s Used: Real Lab Impact

    The biggest draw of 6-Bromobenzo[D]Oxazole is its broad application potential, but several areas benefit most. In medicinal chemistry, it’s often found at the starting line for new bioactive heterocycles. Complex molecules that end up as enzyme inhibitors or receptor modulators frequently begin with scaffold modifications on structures like benzo[d]oxazole. Having a bromo atom in that context becomes a powerful handle for downstream chemistry, particularly for C–C, C–N, or C–O bond formation.

    In material science, these types of heterocycles enter the conversation during synthesis of organic semiconductors, dyes, or pigments. The structure, containing both an electron-rich heterocycle and a halogen substituent, influences the way molecules pack and interact in solid or solution states. In one collaboration with a polymer chemist, integrating this reagent simplified the creation of benzoxazole-based polymers without requiring harsh reaction conditions or elaborate protection-deprotection schemes.

    Analytical chemists also value 6-Bromobenzo[D]Oxazole as a starting reference standard or as a derivatizing agent. Having a compound that dissolves predictably in common organic solvents and withstands both acidic and basic workups enables more flexible protocol design. One project involved quantifying trace analytes in pharmaceutical intermediates; switching to this reagent cut down sample prep time while increasing accuracy.

    Learning from the Competition: Choice Makes a Difference

    Imagine a project facing delays from a stubborn cross-coupling step. In past work, substituting 6-bromoindole for 6-Bromobenzo[D]Oxazole led to unpredictable results: side-products surfaced more often, and purification became a marathon. With 6-Bromobenzo[D]Oxazole, cleaner transformations followed, traceable not just by theory but by sand in the flask and numbers on the NMR. The lesson: structural subtleties matter.

    Other bromoaromatics tend to expose weaknesses under oxidative conditions or in large-scale reactions where atmospheric control is less exact. Over time, the stable nature of 6-Bromobenzo[D]Oxazole cuts back waste and expensive troubleshooting. Users don’t just see an improved yield; they feel empowered to push a project forward, confident the chemistry won’t fall apart at scaling phases.

    Why Purity and Consistency Elevate Science

    Chasing purity might sound tedious to some, but small impurities in starting reagents often sneak all the way through multi-step syntheses. One contaminated batch can throw off months of work. With reliable batches of 6-Bromobenzo[D]Oxazole, those headaches shrink. Results tell the story. Better reproducibility leads to stronger publications or patent applications—goals every research group aims for.

    Having trained newer researchers, confidence to focus on experimental design, not sideline troubleshooting, shows up in creative output. Faster progress. More robust data sets. Projects move from bench to paper without months lost tracing sources of error. These incremental wins impact morale and budget, both of which are more valuable than most realize until they're gone.

    Addressing Safety and Sustainability: Real-World Considerations

    Concerns around halogenated reagents sometimes surface, especially regarding waste and environmental impact. In my own lab, adopting 6-Bromobenzo[D]Oxazole didn’t come with increased hazards compared to alternatives. Standard PPE and fume hood work suffice, without resorting to over-the-top protective setups. Material safety data points to low volatility and manageable risk under normal usage.

    On the sustainability front, selective coupling reactions enabled by the structure minimize byproducts. That means less solvent and energy wasted on purification or repeat reactions. In pharmaceutical or fine chemical production, these savings accumulate. Manufacturers dedicated to greener chemistry routines can appreciate the downstream drops in waste generated, providing both an ethical and practical benefit.

    Industry Benchmarks: How 6-Bromobenzo[D]Oxazole Compares

    Some prefer to roll the dice with less expensive intermediates or poorly characterized analogs. My experience tells me this rarely pays off. Cheaper reagents tend to lack batch certification, documentation, or reliable supply—all crucial at project milestones. The chemical industry, especially in high-stakes R&D, puts premiums on security of supply and transparency. Consistent documentation, reliable spectral data, and clear batch tracking back up every purchase.

    The best suppliers for 6-Bromobenzo[D]Oxazole match these standards. Documentation is transparent, and any deviations become clear early in the project, not buried in the appendix of a final report. When a project pivots quickly, immediate access to new lots or technical support can be the difference between meeting a deadline and missing a publication cycle.

    Next Steps and the Bigger Picture

    6-Bromobenzo[D]Oxazole doesn’t just fill a space on the storeroom shelf. Any research chemist pushing the boundaries of discovery stands to benefit from adaptable, dependable starting materials. For those involved in structure-activity optimization, combinatorial library synthesis, or early hit-to-lead development, a streamlined path toward new analogs from a single, reliable reagent clears away so many of the day-to-day frustrations of lab life.

    Having spent time wrestling with less reliable alternatives, it’s clear that this compound offers more than just an incremental improvement. Its robust, adaptable nature and proven performance in cross-coupling, substitution, and material design free researchers to focus on the big questions—leaving less to chance and cutting routine troubleshooting off at the source.

    Supporting Scientific Discovery Across Disciplines

    Pharmaceutical and agrochemical sectors put a premium on efficiency, patentability, and regulatory compliance. Having a bromoheterocycle on hand that stands up to scrutiny helps teams accelerate programs without running into surprise setbacks during late-stage synthetic modification. Medicinal chemists, often tasked with generating dozens of analogs on tight timelines, end up spending less time on optimization and more on actual discovery once 6-Bromobenzo[D]Oxazole enters their workflow.

    Beyond human health applications, polymer chemists working on next-generation electronic materials or high-performance coatings also benefit. The balance between electron-rich and electron-accepting components in this molecule helps finetune material properties that ultimately wind up in displays, sensors, or solar panels. In those cases, precise control over molecular substitution leads to higher-performing, more robust products down the line.

    The Real-World Researcher’s Perspective

    Every seasoned chemist keeps mental notes on which reagents rescue a struggling project. From hands-on experience across both small academic setups and larger industrial organizations, 6-Bromobenzo[D]Oxazole sits high atop that list. Reproducibility gives peace of mind. Reliable documentation smooths collaboration between teams and across continents. Stable physical properties reduce spillage and decay. All these go far in supporting both small-scale innovation and large-batch consistency.

    Every hour spent troubleshooting an erratic, impure reagent is an hour stolen from creative inquiry. Those numbers add up, especially for new students just learning the ropes or seasoned chemists tasked with overseeing multiple projects simultaneously. By focusing on reagents with track records for quality and reliability, labs set themselves up for fewer surprises—and more breakthroughs.

    Addressing the Challenges: Progress for the Chemistry Community

    The pace of innovation in chemical synthesis depends heavily on foundations built by reliable reagents. As projects grow more ambitious—moving beyond simple aromatic substitutions toward multi-functionalized, stereochemically rich targets—having control at every step turns into a key competitive edge. The industry-wide shift toward open data, traceable sourcing, and third-party auditing reflects a desire for robust, reproducible science, and products such as 6-Bromobenzo[D]Oxazole fit naturally into this landscape.

    Chasing down exotic intermediates can lead to last-minute procurement emergencies. From years in the field, investing upfront in trusted, well-documented reagents often spells the difference between success and missed opportunity. Ensuring projects stay on track, on-budget, and on-time has driven countless chemists to revisit their procurement priorities. With this benzoxazole derivative, the trade-off between cost and value tilts strongly toward the long-term benefit.

    Putting It All Together: The Human Side of Chemistry

    Good science relies on both people and materials. 6-Bromobenzo[D]Oxazole, though just one part of a much bigger picture, plays a role that ripples through project timelines, lab budgets, and team morale. Walking into a team meeting having solved a challenging synthetic transformation thanks to a reliable building block helps create trust across research groups and stakeholders.

    The difference between a reagent that ‘just works’ and one that falls short echoes across the working day—from the first coffee-fueled planning session in the morning, through the daily round of experiments and analyses, to closing up shop at night. Reliable, versatile products like 6-Bromobenzo[D]Oxazole help research teams shift their time and energy from patching problems to asking bigger questions. And in a world where innovation moves quickly and resources are always stretched, those advantages don’t just matter—they determine success.