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Methyl 2-Chloro-4-(Trifluoromethyl)Pyrimidine-5-Carboxylate

    • Product Name Methyl 2-Chloro-4-(Trifluoromethyl)Pyrimidine-5-Carboxylate
    • Alias Methyl 2-chloro-4-(trifluoromethyl)-5-pyrimidinecarboxylate
    • Einecs 629-819-6
    • 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

    305465

    Chemical Name Methyl 2-Chloro-4-(Trifluoromethyl)Pyrimidine-5-Carboxylate
    Cas Number 134098-61-6
    Molecular Formula C7H4ClF3N2O2
    Molecular Weight 240.57
    Appearance White to off-white solid
    Melting Point 64-68°C
    Solubility Slightly soluble in water; soluble in organic solvents
    Purity Typically ≥98%
    Smiles COC(=O)c1cnc(C(F)(F)F)nc1Cl
    Inchi InChI=1S/C7H4ClF3N2O2/c1-15-6(14)3-12-5(2-13-7(3)8)4(9,10)11/h2H,1H3
    Storage Conditions Store at 2-8°C, in a dry and well-ventilated area
    Hazard Class Irritant

    As an accredited Methyl 2-Chloro-4-(Trifluoromethyl)Pyrimidine-5-Carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 25 grams, with tamper-evident cap and hazard labeling; marked with compound name, purity, and safety information.
    Shipping Methyl 2-Chloro-4-(Trifluoromethyl)Pyrimidine-5-Carboxylate is shipped in secure, airtight containers to prevent moisture and contamination. It is packed and labeled following hazardous chemical transport regulations. Shipping typically requires temperature control and careful handling to ensure chemical stability and safety during transit. Documentation accompanies each shipment for regulatory compliance.
    Storage Methyl 2-Chloro-4-(Trifluoromethyl)Pyrimidine-5-Carboxylate 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 or as specified by the manufacturer. Ensure proper chemical labeling and restrict access to trained personnel only.
    Application of Methyl 2-Chloro-4-(Trifluoromethyl)Pyrimidine-5-Carboxylate

    Applications of Methyl 2-Chloro-4-(Trifluoromethyl)Pyrimidine-5-Carboxylate in Industrial Manufacturing

    As an established manufacturer of advanced pyrimidine derivatives, we provide Methyl 2-Chloro-4-(Trifluoromethyl)Pyrimidine-5-Carboxylate to companies operating in highly specialized synthesis-driven sectors. Our production supports essential transformations in pharmaceutical, agrochemical, and specialty intermediate manufacture, where industry regulations and downstream consistency determine success. We strictly ensure supply chain traceability and batch uniformity, allowing our partners to qualify raw material input for their demanding processes.

    1. Pharmaceutical API Intermediate Synthesis

    Pharmaceutical manufacturers employ this compound as a pyrimidine building block in multi-step synthesis of active pharmaceutical ingredients, particularly in the production of kinase inhibitors and antiviral drugs. The material goes through a strictly controlled integration phase in which it reacts with amines, hydrazines, or heterocyclic nucleophiles. Downstream partners perform quality audits on all incoming lots before introducing the raw material early in heterocyclic ring modifications. Adjustments to addition rates depend on the nature of the subsequent substitution or coupling step, impacting both yield and impurity profile management according to the latest ICH and cGMP guidelines.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monograph standards for API intermediates
    • US FDA 21 CFR Parts 210/211 requirements for pharmaceutical manufacturing
    • Japanese Pharmacopoeia (JP) traceability and impurity control

    Typical usage ratio

    • 0.8–1.2 molar equivalents based on targeted API batch size; precise dosage tailored to downstream reactivity and stoichiometry of core coupling reaction

    Downstream process integration

    • Input stage for nucleophilic aromatic substitution or amidation, after solvent charge and prior to subsequent coupling

    Final product types

    • Pharmaceutical drug substance (intermediate and advanced)
    • Final APIs for oncology and antiviral therapeutics

    2. Agrochemical Active Ingredient Precursor

    Crop protection chemical manufacturers use our pyrimidine derivative as a precursor for herbicide and fungicide actives, taking advantage of its electron-deficient aromatic core for downstream functionalization. Process engineers adjust concentration based on the targeted agrochemical class, introducing the compound into heterocyclic cyclization or fluorination steps, often under inert conditions. High purity and low residual moisture ensure consistent reactivity for large-scale production of triazole and pyrimidinone pesticide molecules, where process and environmental regulations dictate trace-level contaminant specifications.

    Industry compliance standards

    • FAO/WHO Specifications for Agricultural Pesticides
    • ISO 9001:2015 Quality Management Systems
    • REACH (EC 1907/2006) chemical registration for pesticide intermediates
    • Chinese National Standards for Agrochemical Synthesis (GB/T series)

    Typical usage ratio

    • 10–25% w/w in reaction charge; modified by targeted molecule’s substitution pattern and yield optimization studies

    Downstream process integration

    • Core intermediate introduction after deprotection or halogenation, in continuous stirred-tank reactors or batch synthesis prior to formulation

    Final product types

    • Technical concentrate of herbicides
    • Systemic fungicide ingredients

    3. Fluorinated Fine Chemical Intermediate Manufacturing

    Manufacturers of specialty fluorinated compounds incorporate our material as a key functionalized pyrimidine for synthesizing advanced electronic materials and performance coatings. The trifluoromethyl and chloro substituents promote desirable reactivity in stepwise fluorination, cross-coupling, and hydrolysis stages. Addition rates depend on both the required substrate conversion and downstream product functional density, with fine-tuning conducted in pre-pilot trials to confirm end-use performance and regulatory shelf-life requirements.

    Industry compliance standards

    • ISO 14001 Environmental Management in fine chemical processing
    • UL and RoHS for electronics and coating applications
    • REACH Annex XVII restriction compliance for fluorinated intermediates
    • Chinese Chemical Industry Standard (HG/T)

    Typical usage ratio

    • 5–15% w/w relative to overall batch size; adjusted according to conversion rates and purity targets for specialty intermediates

    Downstream process integration

    • Intermediate fed into multistep fluorination or cross-coupling reactions, immediately following solvent and catalyst loading

    Final product types

    • Fluorinated specialty oligomers
    • Functional monomers for advanced resins and coatings

    4. Custom Synthesis for Research & Development Applications

    High-purity batches cater to R&D divisions in pharmaceutical, agrochemical, and specialty chemical research organizations. The compound enables rapid construction of new heterocyclic libraries and lead molecule analogs for structure-activity relationship investigations. Research chemists typically use lower charge ratios in parallel synthesis or microwave-assisted protocols, balancing scalability with reactivity screening under laboratory safety and environmental protection standards.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • ISO/IEC 17025 for analytical and calibration laboratories
    • Internal QA/QC protocols of research institutions
    • REACH pre-registration for R&D uses

    Typical usage ratio

    • 0.05–1.0 mmol scale per reaction; ratio depends on desired product library size and the scope of structure-activity studies

    Downstream process integration

    • Weighing and charging during parallel reaction screening, prior to automated purification or workup

    Final product types

    • Reference standards for pharmaceutical and agrochemical research
    • Analytical intermediates for new heterocyclic compound libraries
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