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5-Bromo-Benzooxazole

    • Product Name 5-Bromo-Benzooxazole
    • Alias 5-Bromobenzo[d]oxazole
    • Einecs 620-043-6
    • 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
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    410244

    Productname 5-Bromo-Benzooxazole
    Casnumber 17412-73-2
    Molecularformula C7H4BrNO
    Molecularweight 198.02 g/mol
    Appearance White to off-white solid
    Meltingpoint 114-117 °C
    Purity Typically ≥ 98%
    Solubility Soluble in organic solvents (e.g., DMSO, dichloromethane)
    Smiles Brc1ccc2ocnc2c1
    Inchi InChI=1S/C7H4BrNO/c8-5-1-2-6-7(3-5)9-4-10-6/h1-4H

    As an accredited 5-Bromo-Benzooxazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 5-Bromo-Benzooxazole is packaged in a 25-gram amber glass bottle with a tamper-evident screw cap and clear labeling.
    Shipping **5-Bromo-Benzooxazole** is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It is typically transported via ground or air in compliance with relevant chemical safety regulations, such as IATA and DOT. Proper labeling and documentation ensure safe and legal transit. Handle with caution during receipt and storage.
    Storage 5-Bromo-Benzooxazole should be stored in a tightly sealed container, protected from light and moisture. It should be kept in a cool, dry, and well-ventilated area away from sources of ignition, heat, and incompatible substances such as strong oxidizers. Proper laboratory chemical storage protocols, including appropriate labeling and secondary containment, should be followed to ensure safety and chemical integrity.
    Application of 5-Bromo-Benzooxazole

    Applications of 5-Bromo-Benzooxazole in Industrial Manufacturing

    5-Bromo-Benzooxazole serves as an essential intermediate in several specialized chemical manufacturing processes, primarily in sectors that demand high-purity heterocyclic building blocks. Our manufacturing team focuses on downstream applications where material performance and regulatory adherence drive value for formulators, integrators, and end-use producers.

    1. Pharmaceutical Active Ingredient Synthesis

    This compound plays a fundamental role in advanced heterocycle construction for specialty pharmaceutical actives, particularly in therapeutic classes where benzooxazole scaffolds enhance biological activity. Its integration into the early steps of API synthesis supports the production of both clinical-stage and commercial molecules, often where selectivity, purity, and ionizable halogens are essential for molecular elaboration. Manufacturers utilize this intermediate in small-molecule synthesis pipelines focused on cancer therapeutics and central nervous system agents, especially when exploring structure–activity relationships in benzo-fused heterocycles.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU Guidelines for Good Manufacturing Practice for Medicinal Products for Human and Veterinary Use
    • US FDA’s 21 CFR Part 211
    • Chinese Pharmacopoeia (ChP) for API intermediates

    Typical usage ratio

    • Applied at 0.12–0.25 moles per mole of target benzooxazole core; precise loading varies by API route optimization and targeted impurity profile, with strict in-process monitoring

    Downstream process integration

    • Direct involvement in stepwise heterocycle assembly, commonly via Suzuki–Miyaura or Buchwald–Hartwig cross-coupling, often under anhydrous inert atmosphere, preceding final dehalogenation or amination stages

    Final product types

    • Small-molecule APIs for oncology, anti-infective, and CNS indications
    • Advanced research intermediates subjected to further derivatization programs

    2. Electronic Display Material Synthesis

    Manufacturers in optoelectronic material supply chains employ this brominated heterocycle to construct benzooxazole-based ligands and core fragments required in organic electronic and OLED display architectures. The electron-withdrawing bromine supports the induction of charge-transport properties when integrated in polymeric semiconductors, especially within light-emitting layers where purity and predictable reactivity prevent color shift or device instability. Precise compositional control helps maintain tight device-to-device emission specifications in mass production.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems (specialty electronics)
    • RoHS Directive (2011/65/EU) for hazardous materials in electronic devices
    • IEC 61249-2-21 for halogen content in base materials

    Typical usage ratio

    • Utilized at 1–5 wt% in monomer feedstock formulation, with final quantity adjusted to optimize layer mobility and emission efficiency in thin-film deposition

    Downstream process integration

    • Enters as a key monomer for polymerization or as palladium-coupling precursor during synthesis of benzooxazole-based hole- or electron-transport materials; subsequent purification achieves low ionic contaminant profile necessary for device fabrication

    Final product types

    • OLED display panel emitters and transport layers
    • Organic photodetector materials
    • Semiconductor polymer resins for flexible electronics

    3. Agrochemical Intermediate Manufacturing

    Crop protection chemical producers select this building block for the synthesis of complex benzo-fused heterocycles required in new-generation herbicides, fungicides, and insecticidal actives, where site-specific functionalization determines target binding and environmental fate. Manufacturers appreciate the controlled reactivity of the bromo substituent during multistep routes to deliver biocidal moieties while managing side reactions that could influence ecological risk or toxicity profiles. Formulation teams utilize the intermediate where regulatory scrutiny on purity and trace contaminant levels is most stringent.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • ISO 9001:2015 for quality assurance in agrochemical manufacturing
    • REACH (EC 1907/2006) registration and notification for intermediates
    • EPA 40 CFR Parts 152–180 (US regulations for pesticide manufacturing)

    Typical usage ratio

    • Incorporated at 0.08–0.19 molar equivalents in route design, with variations driven by route efficiency, targeted substitution pattern, and cost controls for multi-ton production

    Downstream process integration

    • Integrated after halogen–metal exchange, Suzuki coupling, or direct nucleophilic substitution; careful in-process chromatography and distillation maintain impurity levels below regulatory cut-offs

    Final product types

    • Systemic fungicides based on benzooxazole derivatives
    • Selective herbicide actives for cereal and rice crops
    • Specialty seed treatment agents

    4. Specialty Dye and Optical Brightener Manufacturing

    Producers of fluorescent dyes and performance optical brighteners introduce this material into aromatic coupling protocols, exploiting the selectivity of the bromo group to modulate chromophore resonance and photostability. Manufacturers rely on this intermediate to fine-tune emission wavelengths in final dye products for applications in high-performance textile whitening and anti-counterfeiting security inks, where precise absorption and re-emission profiles matter for product acceptance and specification compliance. Stringent raw material controls are maintained given the downstream end-market sensitivity.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management Systems
    • OEKO-TEX® Standard 100, Annex 4 (in textile applications)
    • REACH SVHC screening (EU regulations)
    • ISO 18314-1:2015 (Analytical performance of colorants and optical whiteners)

    Typical usage ratio

    • Ranges from 0.10–0.25 molar equivalents relative to coupling partner, with small upward adjustment possible depending on desired extinction coefficient or whiteness index in the formulated optical brightener

    Downstream process integration

    • Introduced post-nitration or amidation phase, forming part of a key condensation or oxidative coupling step; post-reaction work-up includes recrystallization to decorative-grade purity

    Final product types

    • Optical brighteners for synthetic fiber and laundry products
    • Security pigments for anti-counterfeit marking
    • Photostable fluorescent dyes for textile and plastic applications
    Free Quote

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