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2-(3,4-Difluorophenyl)Indole

    • Product Name 2-(3,4-Difluorophenyl)Indole
    • Alias AKOS016256030
    • Einecs 'EINECS 695-935-5'
    • 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

    231795

    Chemical Name 2-(3,4-Difluorophenyl)indole
    Molecular Formula C14H9F2N
    Molecular Weight 229.23
    Cas Number 924835-53-2
    Appearance Off-white to light yellow solid
    Melting Point 162-164°C
    Purity Typically ≥98%
    Solubility Slightly soluble in organic solvents (e.g., DMSO, DMF)
    Smiles C1=CC=C2C(=C1)C=CN2C3=CC(=C(C=C3)F)F
    Inchi InChI=1S/C14H9F2N/c15-11-6-7-12(16)13(10-11)14-9-17-8-5-3-1-2-4-8/h1-7,9-10,17H
    Storage Temperature 2-8°C

    As an accredited 2-(3,4-Difluorophenyl)Indole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 2-(3,4-Difluorophenyl)Indole is packaged in a 10g amber glass bottle with a tamper-evident seal and clear labeling.
    Shipping 2-(3,4-Difluorophenyl)Indole is securely packed in sealed, chemical-resistant containers to prevent contamination and degradation. Shipments comply with all relevant safety regulations, including labeling for hazardous materials if applicable. Packaging ensures protection from moisture, light, and physical damage during transit, and includes appropriate documentation for safe and legal delivery.
    Storage 2-(3,4-Difluorophenyl)indole should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizing agents. Store at room temperature and avoid moisture exposure. Properly label the container and ensure access is restricted to trained personnel. Always follow local regulations and safety guidelines for chemical storage.
    Application of 2-(3,4-Difluorophenyl)Indole

    Applications of 2-(3,4-Difluorophenyl)Indole in Industrial Manufacturing

    As the direct manufacturer of 2-(3,4-Difluorophenyl)Indole, we tailor our raw material supply for specialized industries where performance, traceability, and process compatibility can be quantitatively validated. The following application scenarios highlight established industrial uses based on regulatory standards, technical production integration, precise formulation ranges, and real-world end products.

    1. Pharmaceutical Intermediates for Anticancer APIs

    Leading pharmaceutical plants use this compound as a key intermediate in the synthesis of indole-based kinase inhibitors, which target aberrant protein signaling in oncology therapies. Manufacturers adhere to international pharmacopoeia and GMP requirements to enable final API approval. Material introduction takes place during the targeted heterocyclic coupling stage, directly impacting molecular structure and final product purity.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practices for APIs
    • European Pharmacopoeia (Ph. Eur.) monographs on synthetic intermediates
    • FDA 21 CFR Part 211 for finished pharmaceuticals
    • WHO GMP guidelines for chemical synthesis

    Typical usage ratio

    • 0.3 – 0.7 molar equivalents relative to target kinase inhibitor scaffold; the precise ratio depends on the substitution profile required for the active pharmaceutical ingredient.

    Downstream process integration

    • Material is charged during palladium-catalyzed cross-coupling in Stage II or III of the total synthesis route, after protecting group removal and pre-cursor validation.

    Final product types

    • Approved active pharmaceutical ingredients (APIs) for Phase II/III oncology drugs
    • Reference standards for clinical research compounds
    • Bulk intermediates for CDMO contract API manufacture

    2. Agrochemical Discovery and Seed Treatment Formulations

    Major agrochemical producers employ the raw material in structure-activity relationship (SAR) driven modification of strobilurin or indole-class fungicides. The compound enables precise fluorination in target molecule backbones, improving fungicidal stability and field persistence. Quality control teams monitor incorporation and adjust formulation parameters based on desired active content.

    Industry compliance standards

    • OECD Series on Testing and Assessment No. 107–129 for chemical characterization
    • FAO/WHO specifications for plant protection products
    • ISO 17025 for laboratory testing of pesticide actives
    • EPA 40 CFR Part 180 for pesticide tolerances

    Typical usage ratio

    • 0.1 – 2.5% weight percent in wettable powder or suspension concentrate, determined by SAR optimization trials and final field trial results.

    Downstream process integration

    • Introduced at the lead optimization stage for developing fungicide AI, followed by melt compounding or microencapsulation during final formulation blending.

    Final product types

    • Seed coatings with enhanced disease resistance
    • Fungicide technical concentrates for direct dilution in agricultural supply chains
    • Strobilurin analogues for post-patent agrochemicals

    3. Specialty Organic Electronic Materials

    Leading electronics companies integrate the indole derivative in organic light-emitting diode (OLED) emitters, manipulating charge transfer properties by targeted fluorination. The raw material’s precise crystalline purity and traceability fit strict electronics-grade supply chain requirements, sustaining stable device performance and scale-up reproducibility.

    Industry compliance standards

    • JEDEC industry guidelines for raw material purity in electronics
    • IPC-6012 Class 3 for high-reliability printed electronics
    • RoHS Directive 2011/65/EU with substance documentation
    • REACH Registration and Safety Data registration for EU manufacturing

    Typical usage ratio

    • 0.05 – 0.2 molar equivalents in emitter-host blend formulation; loading tuned to charge transport and device emission layer architecture.

    Downstream process integration

    • Dosed during small molecule vapor deposition for OLED stack fabrication; monitored in situ by material tracking software for roll-to-roll coating or vacuum deposition lines.

    Final product types

    • Blue and green subpixel emitters for OLED panels
    • Organic semiconductors for thin-film transistors (TFTs)
    • Flexible displays and lighting modules containing indole fluorophores

    4. Fine Chemical Synthesis: Fluorinated Heterocycle Building Blocks

    Producers of advanced performance materials use this advanced building block in the multi-step synthesis of high-performance fluorinated heterocycles, often destined for solvent-resistant coatings, specialty adhesives, and custom research reagents. Downstream users require raw material analytics and certificates of analysis to meet project-based QC audits.

    Industry compliance standards

    • ISO 9001:2015 for fine and specialty chemical production
    • SOCMA ChemStewards for batch traceability
    • ECHA REACH pre-registration for chemical intermediate handling
    • Custom Material Safety Data Sheet (MSDS) per final downstream formulation

    Typical usage ratio

    • 1.0 equivalent (stoichiometric) in nucleophilic aromatic substitution or Suzuki coupling; scales from 5 g/L for small-lot R&D to 50 kg/batch in pilot and scale-up production.

    Downstream process integration

    • Charged as a limiting reagent in Stage I/II for construction of fluorinated bicyclic scaffolds, then purified by flash chromatography or crystallization, depending on impurity profile requirements.

    Final product types

    • Custom heterocyclic compounds for contract synthesis clients
    • Precursor components in high-stability engineering polymers
    • Intermediate stocks for research laboratories and technical service centers
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