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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 | 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. |
Applications of Methyl 2-Chloro-4-(Trifluoromethyl)Pyrimidine-5-Carboxylate in Industrial ManufacturingAs 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 SynthesisPharmaceutical 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
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2. Agrochemical Active Ingredient PrecursorCrop 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
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3. Fluorinated Fine Chemical Intermediate ManufacturingManufacturers 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
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4. Custom Synthesis for Research & Development ApplicationsHigh-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
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