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1-Bromo-8-chlorodibenzofuran

    • Product Name 1-Bromo-8-chlorodibenzofuran
    • Alias 8-Chloro-1-bromodibenzofuran
    • Einecs 629-023-6
    • 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

    745254

    Product Name 1-Bromo-8-chlorodibenzofuran
    Cas Number 93777-22-1
    Molecular Formula C12H6BrClO
    Molecular Weight 281.54
    Appearance White to off-white solid
    Melting Point 110-114°C
    Purity Typically >97%
    Solubility Slightly soluble in organic solvents
    Smiles Clc1cccc2oc3ccc(Br)cc3c12
    Inchi InChI=1S/C12H6BrClO/c13-8-5-7-3-1-2-4-10(7)15-12-9(8)6-11(14)12/h1-6H
    Synonyms 1-Bromo-8-chloro-dibenzofuran
    Storage Conditions Store in a cool, dry place, protected from light
    Hazard Statements May cause irritation to skin, eyes, and respiratory tract

    As an accredited 1-Bromo-8-chlorodibenzofuran factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 10 grams of 1-Bromo-8-chlorodibenzofuran, tightly sealed, with clear hazard and identification labeling.
    Shipping 1-Bromo-8-chlorodibenzofuran is shipped in tightly sealed, chemically resistant containers to prevent leaks and contamination. It should be protected from light, moisture, and extreme temperatures. Classified as a hazardous material, it requires proper labeling and handling according to regulatory standards. Only authorized personnel should manage the transport and receipt of this chemical.
    Storage 1-Bromo-8-chlorodibenzofuran should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizers. The storage area should be clearly labeled, free from moisture, and protected from sources of ignition. Personal protective equipment (PPE) is recommended when handling the chemical to avoid exposure.
    Application of 1-Bromo-8-chlorodibenzofuran

    Applications of 1-Bromo-8-chlorodibenzofuran in Industrial Manufacturing

    1-Bromo-8-chlorodibenzofuran serves as a specialized intermediate for advanced chemical synthesis. The material is mainly used by producers in high-value downstream sectors requiring stringent quality, high reactivity, and reproducibility. Below, we present core application scenarios in real-world industries, with an in-depth focus on compliance, formulation, and process integration based on actual manufacturer experiences.

    1. Pharmaceutical Active Ingredient Intermediate Synthesis

    Pharmaceutical manufacturers employ 1-Bromo-8-chlorodibenzofuran as a halogenated building block for the synthesis of certain bioactive compounds, particularly in oncology and anti-infective projects. This intermediate enters catalytic coupling reactions, such as Suzuki or Buchwald–Hartwig protocols, to generate advanced heterocyclic scaffolds. The material's dual halogenation boosts reactivity for regioselective arylation, allowing precise structural derivatization needed to meet API impurity and purity requirements. Pilot and production-scale processes require validated analytical controls to maintain batch quality aligned with regulatory filings.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA cGMP (21 CFR Part 210/211) for drug substance intermediates
    • European Pharmacopoeia monographs for related intermediates
    • REACH registration for substance use in pharmaceutical synthesis

    Typical usage ratio

    • 0.5–1.2 molar equivalents per target API intermediate batch, adjusted to reaction scale and conversion efficiency benchmarks

    Downstream process integration

    • Charged during protected heterocycle coupling, generally after initial substrate activation, under controlled inert atmosphere using specialized catalyst and base systems

    Final product types

    • Advanced pharmaceutical intermediates for clinical development
    • Key building blocks for targeted cancer APIs
    • Precursors to central nervous system (CNS) drug candidates

    2. Organic Electronic Material Precursor

    Within the organic electronics sector, leading component manufacturers utilize this dibenzofuran derivative to produce engineered conjugated molecules for use in OLED (organic light-emitting diode) displays and organic solar cell architectures. The compound’s distinct bromo- and chloro- functionality enables stepwise cross-coupling, affording customized molecular semiconductors with tailored energy band gaps. Consistent supply chain quality is critical for downstream deposition and fabrication, impacting device efficiency and yield.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) compliance for display and lighting applications
    • IEC 61249-2-21 halogen-free material content regulation
    • ISO 9001:2015 Quality Management for precision chemicals

    Typical usage ratio

    • 5–12 wt% based on total organic precursor formulation, optimized for film-forming or layer thickness requirements during spin coating or inkjet printing

    Downstream process integration

    • Introduced post-polymerization for C–C or C–N cross-coupling step, contributing to emissive or charge-transport layer synthesis in multi-staged organic electronic precursor production

    Final product types

    • OLED emitter and host materials
    • Organic photovoltaic (OPV) donor/acceptor materials
    • Thin-film transistor (TFT) semiconductors for display arrays

    3. Agrochemical Discovery and Crop Protection Research

    R&D divisions in agrochemical companies leverage the structural versatility of 1-Bromo-8-chlorodibenzofuran for the generation of new herbicidal and fungicidal candidates. Its unique substitution pattern fits into scaffold-hopping strategies, leading to the synthesis of compounds with novel modes of action. Control over halogenation levels enables fine-tuning for biological screening programs, where milligram to multi-gram scale syntheses support SAR (structure–activity relationship) optimization pipelines.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP) for synthetic intermediate research
    • European Chemicals Agency (ECHA) substance notification for R&D use
    • ISO 17025 accreditation for QC testing in regulated research

    Typical usage ratio

    • 0.8–2.0 molar equivalents depending on target molecule scaffold and substituent diversity requirements

    Downstream process integration

    • Added to discovery-stage synthetic schemes after initial ring formation, supporting rapid analog generation for field trial assessment

    Final product types

    • Lead agrochemical candidates for herbicide and fungicide development
    • Test compounds for mode-of-action elucidation
    • Intermediates for patent-protected chemical crop protection platforms

    4. Specialty Dye and Fluorescent Compound Manufacture

    Producers of advanced dyes and fluorescent sensors integrate this halogenated dibenzofuran as a key intermediate for constructing polycyclic aromatic hydrocarbon systems. Its halide substitution profile assists in achieving desired wavelength absorption and emission properties, particularly in the visible to near-UV range. Precise stoichiometry and controlled substitution preserve the electronic character and quantum yield of the resulting dyes, which must cater to narrow performance tolerances in laboratory and industrial analytical applications.

    Industry compliance standards

    • EN 71-3 Safety standards for materials in laboratory glassware and plasticware
    • ISO 17034 standard for reference material producers
    • REACH Annex XVII for dye and pigment safety in industrial use

    Typical usage ratio

    • 1.0–1.5 equivalents, with batch size and desired fluorescence profile determining exact inclusion

    Downstream process integration

    • Added in the aromatic coupling stage of custom dye synthesis, followed by purification and spectral property validation

    Final product types

    • High-performance dyes for industrial analytical standards
    • Fluorescent tracers for biomedical assays
    • Chromophores for advanced imaging reagents
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