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2-Bromo-4,6-Difluoroanisole

    • Product Name 2-Bromo-4,6-Difluoroanisole
    • Alias 2-Bromo-4,6-difluoro-1-methoxybenzene
    • Einecs 837-920-5
    • 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

    980695

    Productname 2-Bromo-4,6-Difluoroanisole
    Casnumber 885276-41-9
    Molecularformula C7H5BrF2O
    Molecularweight 223.02
    Appearance Colorless to pale yellow liquid
    Boilingpoint 174-176°C at 760 mmHg
    Density 1.674 g/cm3
    Purity Typically ≥97%
    Refractiveindex 1.514
    Smiles COC1=C(Br)C=C(F)C(=C1)F
    Synonyms 2-Bromo-1-methoxy-4,6-difluorobenzene
    Solubility Insoluble in water; soluble in organic solvents
    Flashpoint 60°C
    Ecnumber N/A

    As an accredited 2-Bromo-4,6-Difluoroanisole 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 2-Bromo-4,6-Difluoroanisole, securely sealed with a tamper-evident screw cap.
    Shipping 2-Bromo-4,6-Difluoroanisole is shipped in tightly sealed containers, protected from moisture and light. It should be transported in accordance with relevant chemical and hazardous materials regulations. Ensure proper labeling and documentation during shipping. Avoid sources of ignition and handle with appropriate personal protective equipment to ensure safety during transit.
    Storage **2-Bromo-4,6-Difluoroanisole** should be stored in a tightly sealed container, away from direct sunlight, heat, and sources of ignition. Store in a cool, dry, well-ventilated area, segregated from incompatible materials such as strong oxidizers. Appropriate chemical storage cabinets should be used, and the container should be clearly labeled. Follow all relevant safety and regulatory guidelines.
    Application of 2-Bromo-4,6-Difluoroanisole

    Applications of 2-Bromo-4,6-Difluoroanisole in Industrial Manufacturing

    As a direct manufacturer with advanced fluorination and bromination capabilities, we deliver 2-Bromo-4,6-Difluoroanisole to industry leaders across several specialized chemical sectors. The following application scenarios outline real downstream uses, focusing on precision processes and compliance-driven requirements in each market segment.

    1. Pharmaceutical Intermediate Synthesis for Fluorinated Active Molecules

    Leading pharmaceutical firms select our material as a building block for developing fluorinated heterocycles and aromatic scaffolds used in new active pharmaceutical ingredient (API) discovery. The unique bromo and difluoro substitution pattern supports regioselective coupling reactions in complex molecule synthesis targeting oncology and anti-infective programs. Process chemists leverage its chemical reactivity for Suzuki or Buchwald-Hartwig coupling during late-stage synthesis steps. Batch traceability and contaminant control are maintained throughout, aligning with regulatory submission demands and downstream API release protocols.

    Industry compliance standards

    • Current Good Manufacturing Practices (cGMP, FDA 21 CFR Part 210/211)
    • International Council for Harmonisation (ICH Q7, Q3A/B for impurities)
    • European Pharmacopoeia raw material monograph guidelines (if referenced in technical package)
    • Certificate of Analysis per customer specification including residual solvents (ICH Q3C)

    Typical usage ratio

    • Applied at 0.8–3.5 molar equivalents depending on target molecule ring system and number of introduction sites; exact ratio optimized by R&D chemists for each reaction step

    Downstream process integration

    • Introduced during aromatic substitution/coupling stages—often as one of the final or penultimate steps before molecule deprotection and crystallization

    Final product types

    • Fluorinated intermediates for APIs (e.g., kinase inhibitors, CNS therapeutics, anti-tumor compounds)
    • Regioselective pharmaceutical building blocks sold to contract development and manufacturing organizations (CDMOs)

    2. Agrochemical Intermediate in Heterocyclic Pesticide Synthesis

    Agrochemical manufacturers utilize our material as an essential aryl donor for constructing difluoro-substituted rings in new classes of herbicides, fungicides and insecticides. The molecular handle facilitates Grignard reactions and metal-catalyzed cross-couplings with functionalized pyridines and triazoles, granting access to next-generation actives with improved field stability and target selectivity. Robust handling documentation and batch certification support downstream registration and product stewardship dossiers globally.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticide Active Ingredients (FAO Manual)
    • REACH (EC 1907/2006) substance registration and purity assessment
    • ISO 9001:2015-certified quality management for raw material supplies
    • Global Harmonized System (GHS) SDS for safe transport and use

    Typical usage ratio

    • Used at 1.0–2.2 molar equivalents in active intermediate syntheses; adjusted based on ring-construction efficiency and target substituent density

    Downstream process integration

    • Added as an arylating reagent in the initial stage of heterocycle construction, followed by additional functional group transformations before final formulation

    Final product types

    • Pyridine-based herbicide active ingredients
    • Difluorinated triazole fungicides
    • Specialty insecticide leads (pre-formulation stage)

    3. High-Performance Liquid Crystal Monomer (LCM) Precursor for Display Panels

    Display manufacturers and specialty chemicals suppliers integrate this compound as a key aromatic precursor during custom LCM synthesis. Its electron-withdrawing difluoro and bromo groups enable fine-tuning of birefringence and viscosity in proprietary films for advanced TFT-LCD (Thin-Film Transistor Liquid Crystal Display) technology. Strict product consistency, metal trace content, and low residual solvent levels are validated through our in-house QC for smooth scale-up to high-purity downstream monomers.

    Industry compliance standards

    • RoHS (Restriction of Hazardous Substances Directive, EU 2011/65/EU)
    • IEC 61249-2-21 (in halogen content limits for displays)
    • Supplier-reported analytical validation (NMR, GC-MS traceability)
    • ISO 14001:2015 Environmental Management where applicable to display chemicals

    Typical usage ratio

    • Integrated at 10–45 wt% in the initial LCM synthesis batch; range varies depending on the targeted mesogenic segment and end-use panel optical requirements

    Downstream process integration

    • Used in the early stage of aromatic coupling and etherification to generate core LCM units before custom polymerization and display cell integration

    Final product types

    • Liquid crystal monomers for TFT-LCD panels (in consumer and industrial displays)
    • Birefringent films and aligned substrates for high-resolution screens

    4. Specialty Fluorinated Aromatic Building Block for Material Science R&D

    Researchers and advanced materials developers value this compound as a high-purity fluorinated aromatic for structural modification in new polymers and specialty resins. Applications include tuning dielectric properties for advanced electronics and introducing selective hydrophobicity in coating systems. Material scientists rely on tight manufacturing tolerances and complete impurity profiling for reproducible research, patent submissions, and novel performance property validation.

    Industry compliance standards

    • ASTM D6100 (standard practice for polymer raw material handling and testing)
    • RoHS/REACH registration if scaled to commercial product development
    • ISO 17025-accredited lab analyses for raw material quality
    • Declaration of Conformity to customer research protocol specifications

    Typical usage ratio

    • Used between 2–30 wt% relative to total monomer or oligomer mass; dosage determined by performance screening or proprietary formulation

    Downstream process integration

    • Incorporated in the first-stage monomer synthesis prior to polymerization or copolymerization; sometimes surface-modified for enhanced functional compatibility

    Final product types

    • Experimental high-frequency dielectric polymers
    • Fluorinated polyaryl ether resins
    • Hydrophobic advanced coatings for electronics and optics
    Free Quote

    Competitive 2-Bromo-4,6-Difluoroanisole prices that fit your budget—flexible terms and customized quotes for every order.

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