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2-Bromo-5-Fluorocinnamic Acid

    • Product Name 2-Bromo-5-Fluorocinnamic Acid
    • Alias 2-Bromo-5-fluoro-3-phenylpropenoic acid
    • Einecs 841-395-8
    • 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

    598673

    Productname 2-Bromo-5-Fluorocinnamic Acid
    Casnumber 393780-97-1
    Molecularformula C9H6BrFO2
    Molecularweight 245.04
    Appearance White to off-white solid
    Meltingpoint 161-164°C
    Purity Typically ≥98%
    Smiles C1=CC(=C(C=C1C=CC(=O)O)Br)F
    Inchikey IGDLFTYTPAIFJU-UHFFFAOYSA-N
    Solubility Slightly soluble in water, soluble in organic solvents

    As an accredited 2-Bromo-5-Fluorocinnamic Acid 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 5 grams of 2-Bromo-5-Fluorocinnamic Acid, sealed with tamper-evident cap and labeled for research use.
    Shipping 2-Bromo-5-Fluorocinnamic Acid is shipped in tightly sealed, chemical-resistant containers to prevent contamination and moisture exposure. Handling complies with hazardous materials regulations, including appropriate labeling and documentation. Typically dispatched via ground or air freight, it is packed with cushioning materials, and safety data sheets (SDS) accompany each shipment to ensure safe handling.
    Storage 2-Bromo-5-Fluorocinnamic Acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of heat, ignition, and direct sunlight. Avoid contact with incompatible substances such as strong oxidizers. Store in a chemical storage cabinet, clearly labeled, and keep away from moisture and incompatible materials to ensure safety and compound stability.
    Application of 2-Bromo-5-Fluorocinnamic Acid

    Applications of 2-Bromo-5-Fluorocinnamic Acid in Industrial Manufacturing

    2-Bromo-5-Fluorocinnamic Acid serves as a key intermediate compound in several high-value chemical synthesis sectors. Supplied at high purity by our manufacturing facility, this material integrates directly into the core of multiple downstream formulation and production operations. Below, we detail specific industrial application fields, highlighting process roles, compliance, and formulation details relevant for B2B partners seeking traceable, specification-driven sourcing.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) Synthesis

    Chemical manufacturers use 2-Bromo-5-Fluorocinnamic Acid chiefly as a halogenated aromatic building block in the synthesis of targeted APIs, especially within heterocyclic drug lead series where selective fluorination and bromination are required for bioactivity modulation. Downstream integrators demand batch-to-batch purity, reagents suitable for regulatory scrutiny under cGMP environments, and precise profile assurance for later API QC release.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • USP, EP, JP monographs for intermediates (as applicable to the target API)
    • 21 CFR Part 210/211 (US FDA GMP for Drug Products)
    • EDQM TSE/BSE risk assessment guidelines for raw material sourcing

    Typical usage ratio

    • 0.8 - 3.5 molar equivalents per targeted API synthesis reaction step, with the exact charge depending on the stoichiometry of the subsequent coupling or cyclization step and impurity control in process development.

    Downstream process integration

    • Charged during the initial condensation or direct aromatic substitution stage; typically dissolved in polar aprotic solvents with controlled temperature ramping, sometimes using phase-transfer catalysis, feeding directly into cyclization, hydrolysis, or Suzuki coupling.

    Final product types

    • Small-molecule pharmaceutical APIs requiring halogenated cinnamic backbone
    • Advanced pharmaceutical intermediates for clinical trial material supply
    • Chemical reference standards for analytical and impurity QC labs

    2. Raw Material in Agrochemical Actives Manufacturing

    Agrichemical formulators incorporate this compound as a core intermediate for synthesizing advanced fluorinated phenylpropanoid herbicides, fungicides, and growth regulators. The compound delivers necessary reactivity for constructing molecular scaffolds used in field crop protection, meeting stringent material identity and trace impurity requirements set by international regulatory authorities overseeing agro actives production.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 quality management systems for agrochemical production
    • Regulation (EC) No 1107/2009 (EU Plant Protection Products regulation)
    • US EPA 40 CFR Part 158 (Data requirements for pesticide registration)

    Typical usage ratio

    • 1.0 - 2.7 molar equivalents per synthetic transformation, usually dictated by the nature of downstream arylation reactions or for yield maximization during multi-step actives assembly.

    Downstream process integration

    • Loaded during the primary Grignard-type condensation or direct halogenation sequence in multi-kilo batch reactors, facilitating phenyl ring extensions or functional group insertion for subsequent crystallization and micronization steps.

    Final product types

    • Herbicidal actives featuring fluorinated aromatic substructures
    • Pre-formulation technical grade fungicides for further dilution and field formulation
    • Plant growth regulating actives intended for crop yield improvement products

    3. Intermediate in Specialty Material and Polymer Additive Synthesis

    Specialty chemical producers deploy this material in the construction of advanced monomer systems intended for functionalized polymer backbones or high-end additive segments, where halogen/fluorine substitution imparts improved solubility, UV stability, or electronic properties. Rigorous documentation accompanies shipments to support downstream traceability demands in specialty plastics and performance coatings industries.

    Industry compliance standards

    • REACH (EC No. 1907/2006) for polymer intermediates
    • GHS/CLP (Globally Harmonised System of Classification and Labelling of Chemicals)
    • ISO 14001:2015 environmental management for specialty chemical manufacturing
    • ASTM D2569 for halogenated aromatic compounds used in polymer precursors

    Typical usage ratio

    • 2.5 - 7% by weight in monomer packages or up to 15 mol% relative to core backbone monomer, selected based on required functional group density and desired end-use properties.

    Downstream process integration

    • Introduced at the co-monomerization or grafting stage, often under controlled temperature and pressure in substitute-facilitated solution polymerization or melt extrusion; also used in step-growth polymerizations for engineering film intermediates.

    Final product types

    • Advanced engineering plastics with halogen-resistant properties
    • UV-absorbing polymers and optical coatings for electronics and optics
    • Specialty adhesion promoter resins for functional coatings

    4. Chemical Intermediate for Fine Chemical and Laboratory Synthesis

    Contract manufacturers and research facilities use this compound as a highly specific, high-purity intermediate for structure–activity relationship (SAR) exploration, reference substance synthesis, and custom molecule construction. High batch consistency, traceable impurity profiles, and fit-for-purpose documentation enable R&D groups to validate their downstream reaction work for both academic and industrial innovation pipelines.

    Industry compliance standards

    • ISO 17034:2016 General requirements for reference material producers
    • GLP (Good Laboratory Practice) for non-clinical safety laboratory studies
    • Relevant intellectual property statutes regarding synthetic route development
    • Certificate of Analysis (CoA) supporting custom impurity and residual solvent thresholds

    Typical usage ratio

    • 0.2 - 1.8 mmol per reaction, with flexibility based on reaction scale (from milligram bench-stage to kilo-lab batch for scale-up or validation runs).

    Downstream process integration

    • Dosed in single-step or multi-step solution-phase reactions, typically subjected to protection/deprotection, coupling, or metal-catalyzed functionalization, before purification and subsequent analytical characterization or derivatization.

    Final product types

    • Reference compounds for method validation and impurity identification
    • Small-lot specialty fine chemicals for custom synthesis clients
    • SAR library members for medicinal chemistry programs
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