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2-Amino-6-Bromo-3-Formylchromone

    • Product Name 2-Amino-6-Bromo-3-Formylchromone
    • Alias 2-Amino-6-Bromo-3-Formyl-4H-Chromen-4-one
    • Einecs 629-825-3
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    495796

    Chemical Name 2-Amino-6-Bromo-3-Formylchromone
    Cas Number 885-87-2
    Molecular Formula C10H6BrNO3
    Molecular Weight 268.07 g/mol
    Appearance Yellow to orange powder
    Purity Typically >98%
    Melting Point 235-238 °C
    Solubility Slightly soluble in DMSO, sparingly soluble in water
    Storage Conditions Store at 2-8°C, protected from light and moisture
    Synonyms 6-Bromo-2-amino-3-formyl-4H-chromen-4-one

    As an accredited 2-Amino-6-Bromo-3-Formylchromone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White plastic bottle labeled "2-Amino-6-Bromo-3-Formylchromone, 5g, For research use only" with hazard and handling instructions printed.
    Shipping 2-Amino-6-Bromo-3-Formylchromone is shipped in tightly sealed containers, protected from light and moisture. It is packaged according to chemical safety standards, typically in inert, non-reactive materials. Appropriate labeling and documentation accompany the shipment, ensuring compliance with local and international transport regulations for laboratory chemicals. Handle with care.
    Storage 2-Amino-6-Bromo-3-Formylchromone should be stored in a tightly sealed container, away from light, heat, and moisture, in a cool, dry, well-ventilated area. Keep it separate from incompatible substances such as strong oxidizers. Store at room temperature or as indicated on the safety data sheet. Always ensure proper chemical labeling and restrict access to authorized personnel only.
    Application of 2-Amino-6-Bromo-3-Formylchromone

    Applications of 2-Amino-6-Bromo-3-Formylchromone in Industrial Manufacturing

    2-Amino-6-Bromo-3-Formylchromone serves as a key intermediate in several specialized industrial sectors. As an original manufacturer, we support its integration into advanced synthetic routes where high purity and consistent quality play a central role. Here, we outline application scenarios that reflect genuine downstream use, with specific compliance requirements, formulation guidelines, process methods, and resultant product categories.

    1. Active Pharmaceutical Ingredient (API) Synthesis for Anticancer Compounds

    Pharmaceutical companies utilize 2-Amino-6-Bromo-3-Formylchromone as a heterocyclic building block for developing novel anticancer agents, prominently within experimental kinase inhibitor research and preclinical development. The material’s unique substitution pattern enables researchers to introduce critical functionalities during the lead optimization stage, directing synthesis via Suzuki or Buchwald–Hartwig coupling steps, frequently after formyl group derivatization.

    Industry compliance standards

    • ICH Q7 Guideline — Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 — US cGMP for Finished Pharmaceuticals
    • EU GMP Part II (APIs)
    • Chinese Pharmacopoeia (preclinical API intermediates)

    Typical usage ratio

    • 0.1–0.8 molar equivalents in small-molecule API intermediate syntheses, adjusted according to target compound design and required substituent position.

    Downstream process integration

    • Engaged during early-stage combinatorial synthesis, typically as a core aromatic substrate in palladium-catalyzed coupling reactions, and further processed through protection/deprotection or selective reduction steps before isolation of active pharmaceutical intermediates.

    Final product types

    • Kinase inhibitor preclinical candidates
    • Chromone-based cytotoxic drug intermediates
    • Molecule libraries for oncology pipeline screening

    2. Fine Chemical Synthesis — Agrochemical Intermediates

    Leading agrochemical manufacturers employ this compound as a functionalized scaffold in the creation of novel fungicide or plant growth regulator intermediates. Its bromo and amino functionalities facilitate subsequent halogen-dance reactions, accessing chromone derivatives with targeted bioactivity. This utility supports scalable process development for registration batch manufacture.

    Industry compliance standards

    • ISO 9001:2015 — Quality Management Systems for Agrochemical Manufacturing
    • FAO/WHO Specifications for Plant Protection Products (intermediate stage)
    • REACH Regulation (EC 1907/2006) Registration for intermediate status

    Typical usage ratio

    • 5–20% w/w in solution-phase intermediate coupling reactions, modulated according to downstream active ingredient structural requirements.

    Downstream process integration

    • Introduced in initial ring-construction reactions, followed by stepwise halogenation or amination to deliver pro-ligand structures suitable for further derivatization into active crop protection molecules.

    Final product types

    • Fungicide pre-intermediates
    • Herbicide structural scaffolds
    • Plant growth regulator precursors

    3. Advanced Organic Pigment and Dye Intermediate Manufacturing

    Producers of specialty pigments incorporate 2-Amino-6-Bromo-3-Formylchromone to create chromone-based dye precursors, especially where extended conjugation and site-specific electron-donating properties are required. The formyl group confers selective reactivity for subsequent condensation or azo-coupling approaches, providing tunable chromatic characteristics.

    Industry compliance standards

    • ISO 9001:2015 — Quality Systems for Organic Pigment Production
    • EN 71-3:2019 — Safety of Toys (Migration of Certain Elements, Pigments applications)
    • Eco Passport by OEKO-TEX® — Textile Chemical Safety (dye intermediates)

    Typical usage ratio

    • 2–10% w/w within pigment intermediate synthesis recipes; adjusted depending on desired dye shade and reactivity with diazonium salts.

    Downstream process integration

    • Employed in the condensation stage for constructing extended chromone-based aromatic rings, or coupled with diazonium compounds for azo pigment formation, prior to purification and pigment stabilization.

    Final product types

    • High-performance chromone-derived pigments
    • Synthetic dyes for inks and plastics
    • Specialty colorants for technical textiles

    4. Specialty Chemical Manufacturing — Analytical Reagents

    Chemical reagent suppliers employ this material for manufacturing chromone-based analytical standards and fluorescent probes. Its molecular framework enables tailored immobilization onto silica supports or integration into sensor arrays, where both the bromine and amino groups serve as anchor points for further modification, supporting analytical device calibration and method development.

    Industry compliance standards

    • ISO/IEC 17025 — General Requirements for the Competence of Testing and Calibration Laboratories
    • Certificate of Analysis (CoA) per laboratory reagent standards
    • RoHS Directive 2011/65/EU (where applicable for electronics-related reagents)

    Typical usage ratio

    • 0.05–1.5% (w/v) in reagent matrix, adjusted by molar response or target detection sensitivity requirements.

    Downstream process integration

    • Employed at the post-synthesis modification stage for probe molecule conjugation, covalent attachment onto immobilized supports, or reacted with luminophores to yield custom chromone-based detection agents.

    Final product types

    • Spectroscopic standards for analytical labs
    • Specialty fluorophores for protein labeling
    • Calibration reagents for chromatography systems
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