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6-Bromo-3-Cyanochromone

    • Product Name 6-Bromo-3-Cyanochromone
    • Alias 6-Bromo-4-oxo-4H-1-benzopyran-3-carbonitrile
    • Einecs 629-392-4
    • 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

    497307

    Productname 6-Bromo-3-Cyanochromone
    Molecularformula C10H4BrNO2
    Molecularweight 250.05 g/mol
    Casnumber 261715-49-1
    Appearance Light yellow solid
    Meltingpoint 215-218°C
    Purity Typically >98%
    Solubility Slightly soluble in organic solvents
    Storageconditions Store at room temperature, in a dry place, and protected from light

    As an accredited 6-Bromo-3-Cyanochromone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle labeled "6-Bromo-3-Cyanochromone, 5g." Features hazard symbols, product code, batch number, and manufacturer's details.
    Shipping 6-Bromo-3-Cyanochromone is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It is classified as a laboratory chemical and may require special handling and labeling. Shipping follows appropriate safety regulations, such as those for hazardous materials, ensuring secure transport to prevent leaks, spills, or exposure during transit.
    Storage 6-Bromo-3-Cyanochromone should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from light and moisture. Keep it away from incompatible substances such as strong acids, bases, and oxidizers. Store at room temperature or as indicated on the label. Properly label the container and ensure restricted access to trained personnel only.
    Application of 6-Bromo-3-Cyanochromone

    Applications of 6-Bromo-3-Cyanochromone in Industrial Manufacturing

    6-Bromo-3-Cyanochromone serves as a strategic intermediate in several downstream chemical manufacturing sectors. As a chemical raw material manufacturer, we maintain strict adherence to regulatory standards and process controls at every stage of production. Below are major industrial application scenarios where our clients integrate this compound into their manufacturing pipelines, detailing compliance, usage ratios, technical processing, and the typical finished goods.

    1. Pharmaceutical API Intermediate in Oncology Drug Synthesis

    Regulated pharmaceutical manufacturers employ 6-Bromo-3-Cyanochromone as a key intermediate for synthesizing anticancer active pharmaceutical ingredients, especially within the class of substituted chromones. The material’s dual-functionality enhances the reactivity required in pyrone ring derivatization and nucleophilic substitution steps. In practice, consistency in purity profiles and trace analysis for residual bromide or cyano moieties fall under GMP-controlled validations. Drug formulators adjust chromone loading depending on desired cytotoxicity profile and therapeutic index of the final API.

    Industry compliance standards

    • ICH Q7A Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • EU GMP Annex 8: Sampling of Starting and Packaging Materials
    • USP/NF Monograph Requirements for Related Substances
    • FDA 21 CFR Part 211 for finished pharmaceuticals

    Typical usage ratio

    • 5–15% (w/w) of total reaction mass, optimized per multi-step API route
    • Adjusted according to target API molecular weight and process yield

    Downstream process integration

    • Charged during early-stage condensation or cyclization
    • Used in nucleophilic aromatic substitution for further substitution on the chromone nucleus
    • Critical to final-stage deprotection or ring closure before isolation of the API

    Final product types

    • Oncology drug intermediates (e.g., pyran-based kinase inhibitors)
    • Final anticancer active pharmaceutical ingredients
    • Chemotherapeutic compound libraries for clinical trial supply
    • Reference compounds for pharmaceutical research

    2. Agrochemical Intermediate for Systemic Fungicide Production

    Agrochemical formulators prefer 6-Bromo-3-Cyanochromone for systemic fungicide synthesis, utilizing its reactivity to create pyrone-based active agents. Downstream plants must comply with safety and trace conformity checks for agrochemical grade inputs. Synthesis scales up in batch reactors, with the bromine position serving as a handle for further halogenation, sulfation, or etherification necessary for generating efficient leaf-penetrant agents.

    Industry compliance standards

    • FAO/WHO Specification for Pesticide Active Ingredients
    • ISO 17025 for in-house QC laboratories
    • Regulation (EC) No 1107/2009 on Plant Protection Products
    • China GB 20810—Pesticide Manufacturing Safety and Hygiene

    Typical usage ratio

    • 8–20% (w/w) chromone-based intermediate relative to active ingredient synthesis batch
    • Modified by crop protection target potency

    Downstream process integration

    • Introduced in early-stage nucleophilic displacement
    • Undergoes halogen-metal exchange before further extension or attachment of alkyloxy side chains
    • Processed in jacketed reactors under controlled temperature ramping

    Final product types

    • Systemic fungicides for cereal and rice protection
    • Pyranone-based crop disease inhibitors
    • Formulated agricultural sprays and seed coat agents
    • Strobilurin analogs for wide-spectrum pathogen control

    3. Organic Electronics Intermediate for OLED Materials

    OLED materials manufacturers utilize 6-Bromo-3-Cyanochromone as a precursor for synthesizing high-performance electron-transporting layers. Its chromone scaffold suits cross-coupling reactions and functionalization through Suzuki or Sonogashira techniques, developing solution-processable dyes and emissive materials. Suppliers ensure material traceability to RoHS and REACH compliance, as microelectronic processors conduct sensitive analyses for ion contamination and impurities.

    Industry compliance standards

    • EU REACH Regulation (EC) No 1907/2006
    • RoHS Directive 2011/65/EU for hazardous substances
    • IEC 62474 Material Declaration for Electronic Industry
    • ISO 9001:2015 for specialty chemical manufacturing quality management

    Typical usage ratio

    • 1–5% (w/w) as precursor relative to bulk high-purity solvent and reaction mass
    • Calibrated by intended molecular weight of the target OLED emitter or transport layer

    Downstream process integration

    • Supplied as solid, purified via column chromatography, then dissolved for in situ cross-coupling
    • Acts as central aromatic node in functional monomer synthesis
    • Processed under low-metal catalyst load to minimize trace metal contamination

    Final product types

    • Electron and hole transport layers in OLED panels
    • Organic light-emitting diode emitters for display and lighting sectors
    • Conductive polymers and organic circuitry for flexible electronics
    • Research-grade OLED dye intermediates

    4. Fine Chemical Intermediate for Advanced Dye Manufacturing

    Dye manufacturers select 6-Bromo-3-Cyanochromone for formulation of high-color-strength dyes used in specialty textiles and printing inks. The molecule’s halogen site directs regioselective substitution and extends π-conjugation through coupling reactions, enabling precise hue tuning and improved fastness. Batch records maintain analytical controls by ISO dye standards and ensure complete conversion and safe handling of reactive intermediates.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Dye and Pigment Manufacturing
    • Oeko-Tex Standard 100 for harmful substances
    • EU Regulation (EC) 1907/2006 REACH listing for dyes
    • ZDHC Manufacturing Restricted Substances List (MRSL)

    Typical usage ratio

    • 2–6% (w/w) relative to total aromatic base in dye synthesis
    • Varies with target color intensity and desired molar extinction coefficient

    Downstream process integration

    • Enters diazo coupling or azo condensation reactions for dye backbone creation
    • Involved in direct arylation for lightfast pigment production
    • Refined by solvent extraction and crystallization before blending into proprietary dye formulations

    Final product types

    • Reactive textile dyes for cotton and synthetic fibers
    • Color-fast digital printing inks for industrial and UV applications
    • High-purity organic pigments for plastics and packaging
    • Light-stable specialty dye additives for photographic use
    Free Quote

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