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Atomfair 3-Chloro-5-(trifluoromethyl)-2-pyridinamine C6H4ClF3N2

Description 3-Chloro-5-(trifluoromethyl)-2-pyridinamine ( CAS 79456-26-1 ) is a high-purity heterocyclic compound with the molecular formula C6H4ClF3N2. This specialized chemical features a pyridine core substituted with a chloro group at the 3-position, a trifluoromethyl group at the 5-position, and an amino group at the 2-position, offering unique reactivity for advanced synthetic applications. Ideal for pharmaceutical intermediates, agrochemical research, and material science, this compound is rigorously tested via GC/MS, HPLC, and NMR to ensure ??98% purity. Packaged under inert gas in amber glass vials to ensure stability, it is suitable for nucleophilic substitution reactions, cross-coupling methodologies, and fluorinated building block synthesis. Store…

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Description

Description

3-Chloro-5-(trifluoromethyl)-2-pyridinamine (CAS 79456-26-1) is a high-purity heterocyclic compound with the molecular formula C6H4ClF3N2. This specialized chemical features a pyridine core substituted with a chloro group at the 3-position, a trifluoromethyl group at the 5-position, and an amino group at the 2-position, offering unique reactivity for advanced synthetic applications. Ideal for pharmaceutical intermediates, agrochemical research, and material science, this compound is rigorously tested via GC/MS, HPLC, and NMR to ensure ??98% purity. Packaged under inert gas in amber glass vials to ensure stability, it is suitable for nucleophilic substitution reactions, cross-coupling methodologies, and fluorinated building block synthesis. Store at 2-8??C in a dry environment.

  • CAS No: 79456-26-1
  • Molecular Formula: C6H4ClF3N2
  • Molecular Weight: 196.56
  • Exact Mass: 196.0015103
  • Monoisotopic Mass: 196.0015103
  • IUPAC Name: 3-chloro-5-(trifluoromethyl)pyridin-2-amine
  • SMILES: C1=C(C=NC(=C1Cl)N)C(F)(F)F
  • Synonyms: 3-Chloro-5-(trifluoromethyl)-2-pyridinamine, 3-Chloro-5-trifluoromethyl-2-pyridylamine, DTXSID00345807, EC 401-670-0, DTXCID00296880

Application

3-Chloro-5-(trifluoromethyl)-2-pyridinamine serves as a key intermediate in the synthesis of biologically active molecules, particularly in agrochemicals (e.g., herbicides, insecticides) and pharmaceuticals (e.g., kinase inhibitors). Its trifluoromethyl group enhances lipophilicity and metabolic stability, making it valuable in medicinal chemistry optimization. The compound is also employed in metal-catalyzed cross-coupling reactions to construct complex heterocyclic scaffolds for material science applications.

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