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Trans-2-(4-Chlorophenyl)Vinylboronic Acid

    • Product Name Trans-2-(4-Chlorophenyl)Vinylboronic Acid
    • Alias cis-2-(4-Chlorophenyl)ethenylboronic acid
    • Einecs 401-220-4
    • 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
    VTB
    Specifications

    HS Code

    461076

    Chemical Name Trans-2-(4-Chlorophenyl)Vinylboronic Acid
    Cas Number 1092739-64-2
    Molecular Formula C8H8BClO2
    Molecular Weight 182.42 g/mol
    Appearance White to off-white solid
    Melting Point Approx. 182-186°C
    Purity Typically ≥97%
    Solubility Slightly soluble in water, soluble in polar organic solvents
    Smiles B(C=CC1=CC=C(C=C1)Cl)(O)O

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

    Packing & Storage
    Packing Trans-2-(4-Chlorophenyl)Vinylboronic Acid, 1 gram, supplied in a sealed amber glass vial with tamper-evident cap and labeling.
    Shipping Trans-2-(4-Chlorophenyl)Vinylboronic Acid is shipped in tightly sealed containers to prevent moisture and air exposure. It is packaged in accordance with chemical safety regulations, typically under inert conditions. Shipping complies with local and international transport guidelines for chemicals, ensuring safe handling and delivery. Temperature control may be applied if required.
    Storage **Trans-2-(4-Chlorophenyl)vinylboronic acid** should be stored in a tightly sealed container, protected from moisture and air. Keep it in a cool, dry place, ideally at 2-8°C (refrigerator temperature). Store away from strong oxidizing agents, acids, and bases. Minimize exposure to light and handle under inert atmosphere if possible to maintain stability and prevent degradation.
    Application of Trans-2-(4-Chlorophenyl)Vinylboronic Acid

    Applications of Trans-2-(4-Chlorophenyl)Vinylboronic Acid in Industrial Manufacturing

    Trans-2-(4-Chlorophenyl)Vinylboronic Acid serves as a specialty intermediate in several advanced chemical manufacturing fields. Our production expertise supports downstream partners across pharmaceutical, agrochemical, and advanced material industries. Each downstream sector requires strict adherence to industry standards, precise formulation controls, and reliable integration into proprietary synthesis processes. Below are the main industrial application scenarios for this raw material.

    1. Pharmaceutical Active Ingredient Synthesis

    This material functions as a boronic acid building block in Suzuki-Miyaura cross-coupling reactions, integral to synthesizing targeted APIs such as oncology and anti-viral compounds. Process engineers dose precise quantities to introduce aryl-vinyl structural frameworks, meeting specifications for high-purity endpoints. Batch record validation and impurity profiling follow ICH Q11 guidelines for pharmaceutical intermediates.

    Industry compliance standards

    • ICH Q7 and Q11 for API intermediate controls
    • EU GMP Part II for API starting materials
    • US FDA 21 CFR Part 211 production protocols
    • Japanese PMDA requirements for synthetic intermediates

    Typical usage ratio

    • Applied at 0.8 – 1.2 molar equivalents relative to halide or triflate partners
    • Ratio adjusted based on palladium catalyst turnover efficiency and API complexity

    Downstream process integration

    • Charged during early-stage Grignard or Suzuki coupling steps
    • Integrated via closed-system addition vessels under nitrogen protection
    • Followed by downstream HPLC purification and crystallization

    Final product types

    • Oncology small molecule APIs
    • Anti-viral pharmaceutical ingredients
    • Chiral aryl-vinyl-based pharmaceutical intermediates
    • High-purity drug research compounds

    2. Agrochemical Intermediate Manufacturing

    Chemical processors utilize this molecule for constructing functionalized aryl-vinyl motifs within crop protection agents. It supports palladium-catalyzed coupling steps leading to novel herbicide or fungicide cores. Regulatory submissions require documentation of intermediate identity, traceability, and absence of persistent organic pollutants in compliance with international agrochemical frameworks.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals
    • European Regulation (EC) No 1107/2009 on plant protection products
    • EPA FIFRA manufacturing reporting
    • ISO 17025 accredited laboratory tests for intermediate quality

    Typical usage ratio

    • 0.9 – 1.3 molar equivalents depending on target scaffold substitution
    • Adjusted per batch yield/desired loading on resin-bound syntheses

    Downstream process integration

    • Introduced during tandem coupling or stepwise synthesis of active ingredient pre-cursors
    • Employed in multi-step reactor trains with real-time NMR monitoring

    Final product types

    • Next-generation herbicide actives
    • Fungicide intermediate scaffolds
    • Crop growth regulatory agent cores
    • Seed treatment chemical bases

    3. Electronic Material Precursor Synthesis

    Producers of organic semiconductors and photoactive polymers select this material for introducing defined conjugated units. The boronic acid moiety enables site-specific aryl-vinyl linkage, foundational for constructing high-mobility charge transport layers. Cleanroom synthesis strictly controls solvent residue and heavy metal contamination per electronic grade standards.

    Industry compliance standards

    • IEC 60747 for semiconductor chemical purity
    • ISO 9001:2015 for quality management
    • REACH Regulation (EC) No 1907/2006 compliance
    • RoHS 2 Directive for electronic components

    Typical usage ratio

    • 0.95 – 1.05 molar equivalents for chain-coupling steps
    • Modulated by desired molecular weight and electronic conjugation targets

    Downstream process integration

    • Dispensed into inert-atmosphere coupling reactors
    • Processed with polymerizable monomer feeds for thin-film deposition

    Final product types

    • Organic FET (Field Effect Transistor) layers
    • OLED (Organic Light Emitting Diode) materials
    • Photoresist and etch mask polymers
    • Flexible display active coatings

    4. Fine Chemical Custom Synthesis

    Custom synthesis contract manufacturers use this intermediate for assembling tailored aryl-vinyl functionalities required in specialty fine chemical preparations. The precise reactivity and para-chlorine substitution support high-value product innovation while allowing robust analytical traceability for pharmaceutical, material science, and R&D customers. Documentation complies with regional and customer-specific custom synthesis expectations, including impurity mapping and batch-level trace certifications.

    Industry compliance standards

    • ISO 9001 for lot traceability and documentation
    • OECD GLP (Good Laboratory Practice) for contract synthesis
    • REACH pre-registration and evaluation for new chemical entities
    • Harmonized System (HS) code classification for international shipment

    Typical usage ratio

    • Applied at 0.5 – 2.0 molar equivalents, determined by unique route design
    • Usage depends on step count, coupling site density, and downstream yield optimization

    Downstream process integration

    • Metered in multi-step kilo lab or pilot plant syntheses
    • Employed at key branching points for further diversification or chiral enrichment

    Final product types

    • Pharmaceutical reference standards
    • Research-scale specialty chemicals
    • Material science intermediates
    • High-purity analytical markers
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