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5-Bromo-2,3-Dihydro-1-Benzofuran

    • Product Name 5-Bromo-2,3-Dihydro-1-Benzofuran
    • Alias 5-Bromo-2,3-dihydrobenzofuran
    • Einecs 620-057-9
    • 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

    955624

    Chemical Name 5-Bromo-2,3-Dihydro-1-Benzofuran
    Cas Number 31786-21-1
    Molecular Formula C8H7BrO
    Molecular Weight 199.05 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 97-99°C at 2 mmHg
    Density 1.536 g/cm³
    Purity Typically ≥ 98%
    Smiles Brc1ccc2c(c1)CCO2
    Inchi InChI=1S/C8H7BrO/c9-6-1-2-7-5(3-6)4-8(10-7)11-7/h1-3,8H,4H2
    Refractive Index 1.5880-1.5900

    As an accredited 5-Bromo-2,3-Dihydro-1-Benzofuran 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 25 grams of 5-Bromo-2,3-Dihydro-1-Benzofuran, sealed with a tamper-evident cap and labeled with hazard warnings.
    Shipping 5-Bromo-2,3-Dihydro-1-Benzofuran is shipped in tightly sealed containers under ambient conditions. It is packaged according to chemical safety regulations to prevent leakage or contamination. Standard hazardous material labeling and documentation are provided. Avoid exposure to extreme temperatures, moisture, or direct sunlight during transit. Handle and store in accordance with SDS guidelines.
    Storage Store 5-Bromo-2,3-dihydro-1-benzofuran in a cool, dry, well-ventilated area away from sources of ignition and incompatible materials such as strong oxidizing agents. Keep the container tightly closed and protected from moisture and light. Store in a chemical-resistant, labeled container and follow all local regulations for storage of hazardous chemicals. Use appropriate personal protective equipment when handling.
    Application of 5-Bromo-2,3-Dihydro-1-Benzofuran

    Applications of 5-Bromo-2,3-Dihydro-1-Benzofuran in Industrial Manufacturing

    Our facility produces 5-Bromo-2,3-Dihydro-1-Benzofuran for specialized use as an advanced intermediate in industries requiring reliable quality and strict regulatory compliance. Below, we outline several established applications in key industrial sectors where our technology delivers consistent results for downstream manufacturing.

    1. Pharmaceutical Active Ingredient Synthesis

    Downstream pharmaceutical companies rely on this compound as a core intermediate when constructing specific benzofuran-based drug molecules. Its unique brominated structure enables targeted ring transformations critical for central nervous system and anti-inflammatory compounds, and our supply chain supports stringent batch traceability. Manufacturers integrate this intermediate in controlled multi-step synthetic routes to obtain APIs featuring dihydrobenzofuran motifs.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • USP General Chapter <1121> for Impurities
    • 21 CFR Parts 210/211 (US FDA cGMP for pharmaceuticals)
    • EU EudraLex Volume 4 Annex 8 (Excipients and Intermediates)

    Typical usage ratio

    • 0.25–0.6 molar equivalents relative to target API precursor, depending on synthetic step
    • Reaction charge adjusted based on desired active content and impurity control

    Downstream process integration

    • Added during early-stage nucleophilic substitution or cross-coupling steps in the multi-stage pharmaceutical synthesis
    • Crucial for constructing halogenated benzofuran scaffolds prior to functional core modifications

    Final product types

    • Small molecule APIs for CNS therapeutics
    • Intermediates for anti-inflammatory and analgesic actives
    • Advanced building blocks for benzofuran-based drug candidates in late-phase development

    2. Agrochemical Intermediate Manufacturing

    This material provides a reliable halogenated scaffold for building benzofuran derivatives in modern crop protection chemistry. Agrochemical formulators introduce it as a central intermediate when producing selective herbicides and fungicides, leveraging its bromo-substitution to enhance downstream synthetic efficiency and end-product selectivity. Process control of reactivity and purity remains crucial for consistent performance in large-scale batch operations.

    Industry compliance standards

    • FAO/WHO Technical Specifications for Pesticides (FAO/WHO JMPR and JMPS)
    • OECD Principles of GLP (Good Laboratory Practice)
    • ISO 9001:2015 Quality Management Systems for chemical manufacturing
    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals (EU market)

    Typical usage ratio

    • 0.2–0.8 molar ratio, depending on target agrochemical backbone and intended bioactivity
    • Charge ratio and feed rate tailored to batch or continuous synthesis design

    Downstream process integration

    • Undergoes further halogenation, alkylation or cyclization during intermediate synthesis
    • Introduced during primary assembly of benzofuran rings in herbicide precursor production

    Final product types

    • Precursor compounds for selective herbicides
    • Key intermediates for triazole and strobilurin fungicide synthesis
    • Crop protection active ingredients incorporating benzofuran motifs

    3. Advanced Material Monomer Development

    Manufacturers of specialty polymers and engineered materials utilize the unique reactivity of brominated dihydrobenzofurans when synthesizing performance monomers for coatings and electronic materials. The compound’s molecular structure facilitates selective cross-coupling or functionalization steps, leading to polymeric and oligomeric materials suited for insulating or dielectric layers.

    Industry compliance standards

    • ISO 14001 Environmental Management System (for chemical synthesis of monomers)
    • IEC 61249 (base materials for printed boards in the electronics industry)
    • ANSI/ESD S20.20 (materials for electrostatic discharge control)
    • RoHS Directive (2011/65/EU) for restricted substances in electrical/electronic equipment

    Typical usage ratio

    • 5–15% by weight of total monomer feed, adjusted per target polymer architecture
    • Bulk loading determined by end-use requirements such as dielectric strength or film flexibility

    Downstream process integration

    • Reactive introduction during controlled radical polymerization or step-growth condensation polymer processes
    • Monomer functionalization pre-polymerization via Suzuki or Heck coupling

    Final product types

    • Benzofuran-based specialty polymer resins
    • Insulation films for flexible electronics
    • Protective coatings for high-reliability printed circuit boards

    4. Fine Chemical Building Blocks for Dye and Pigment Synthesis

    Producers of fine chemical intermediates introduce this material during key stages of benzofuranal or bromoarene dye precursor manufacturing. The molecular reactivity facilitates targeted ring transformations, supporting the high-purity needs of pigment and dye production for industrial textiles and specialized ink applications.

    Industry compliance standards

    • ETAD Code of Ethics (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers)
    • OEKO-TEX Standard 100—chemical input for textiles
    • ISO 9001:2015 Quality system for pigment and dye manufacturing
    • GHS/CLP Regulation EC No. 1272/2008 (EU labeling/hazard communication)

    Typical usage ratio

    • 0.1–0.5 equivalent per target dye or pigment skeleton
    • Entry amount tailored to desired color yield, purity, and downstream conjugation reactions

    Downstream process integration

    • Fed during condensation or ring-closure reactions forming chromophore precursors
    • Subjected to regioselective substitution and further derivatization prior to final dye assembly

    Final product types

    • Benzofuran-based industrial dyes for textiles and leathers
    • Organic pigment intermediates for printing inks and coatings
    • Stable colorant precursors with high lightfastness and chroma

    5. R&D Reference Standard for Analytical Chemistry

    Specialty testing laboratories and contract manufacturers use this compound as a certified analytical reference or spiking standard for method development, impurity profiling, and process validation in benzofuran-related synthetic pathways. The well-characterized physical and chemical properties assist in accurate quantitation and validation of trace analysis protocols for diverse industrial matrices.

    Industry compliance standards

    • ISO/IEC 17025 General requirements for the competence of testing and calibration laboratories
    • USP Reference Standards Program
    • Ph. Eur. General Chapter 2.1.7 (Reference Standards in European Pharmacopoeia context)
    • ASTM E29-13—Standard guide for general principles of quantitative analysis by HPLC/GC/MS

    Typical usage ratio

    • 0.01–10 mg/L for instrument calibration and method performance qualification
    • Quantity determined by analytical range, instrument sensitivity, and matrix

    Downstream process integration

    • Direct dissolution or serial dilution for calibration/validation of analytical methods
    • Spike addition for recovery studies in final product quality control release testing

    Final product types

    • Reference working standards for QC/QA labs
    • Certified calibration kits for GC-MS, HPLC, or LC-MS analysis
    • Proficiency test solutions for trace-level quantification in regulated industries
    Free Quote

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