Atomfair Benzenamine, 2-chloro-5-(trifluoromethyl)- C7H5ClF3N

Description 2-Chloro-5-(trifluoromethyl)aniline (CAS No. 121-50-6) is a high-purity aromatic amine derivative with the molecular formula C7H5ClF3N . This compound features a trifluoromethyl group and a chloro substituent on the benzene ring, making it a versatile intermediate in organic synthesis and specialty chemical production. Its unique structure enhances reactivity in electrophilic substitution and coupling reactions, ideal for pharmaceutical, agrochemical, and material science applications. Available in crystalline form with ??98% purity, it is rigorously tested via GC/HPLC to ensure consistency for research and industrial use. Store in a cool, dry place under inert conditions to maintain stability.

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Description

Description

2-Chloro-5-(trifluoromethyl)aniline (CAS No. 121-50-6) is a high-purity aromatic amine derivative with the molecular formula C7H5ClF3N. This compound features a trifluoromethyl group and a chloro substituent on the benzene ring, making it a versatile intermediate in organic synthesis and specialty chemical production. Its unique structure enhances reactivity in electrophilic substitution and coupling reactions, ideal for pharmaceutical, agrochemical, and material science applications. Available in crystalline form with ??98% purity, it is rigorously tested via GC/HPLC to ensure consistency for research and industrial use. Store in a cool, dry place under inert conditions to maintain stability.

  • CAS No: 121-50-6
  • Molecular Formula: C7H5ClF3N
  • Molecular Weight: 195.57
  • Exact Mass: 195.0062613
  • Monoisotopic Mass: 195.0062613
  • IUPAC Name: 2-chloro-5-(trifluoromethyl)aniline
  • SMILES: C1=CC(=C(C=C1C(F)(F)F)N)Cl
  • Synonyms: 3-Amino-4-chlorobenzotrifluoride, 121-50-6, 2-Chloro-5-(trifluoromethyl)aniline, Benzenamine, 2-chloro-5-(trifluoromethyl)-, Fast Orange Salt RD

Application

2-Chloro-5-(trifluoromethyl)aniline is widely used as a key intermediate in the synthesis of dyes, pigments, and agrochemicals. Its electron-withdrawing groups make it valuable in pharmaceutical research for developing bioactive molecules. The compound also serves as a building block in material science for creating advanced polymers and coatings with enhanced chemical resistance.

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