Atomfair 4-Amino-2,6-difluorobenzotrifluoride C7H4F5N

Description 4-Amino-2,6-difluorobenzotrifluoride (CAS No. 123950-44-7) is a high-purity fluorinated aromatic amine with the molecular formula C7H4F5N . This compound, also known as 3,5-difluoro-4-(trifluoromethyl)aniline , is a versatile building block in organic synthesis, particularly in the development of pharmaceuticals, agrochemicals, and advanced materials. Its unique structure, featuring both amino and trifluoromethyl groups on a difluorinated benzene ring, enables precise reactivity for nucleophilic substitutions and cross-coupling reactions. Suitable for researchers and industrial applications, this product is available in >98% purity (GC) with rigorous QC testing to ensure consistency. Store under inert conditions to maintain stability.

Description

4-Amino-2,6-difluorobenzotrifluoride (CAS No. 123950-44-7) is a high-purity fluorinated aromatic amine with the molecular formula C₇H₄F₅N. This compound, also known as 3,5-difluoro-4-(trifluoromethyl)aniline, is a versatile building block in organic synthesis, particularly in the development of pharmaceuticals, agrochemicals, and advanced materials. Its unique structure, featuring both amino and trifluoromethyl groups on a difluorinated benzene ring, enables precise reactivity for nucleophilic substitutions and cross-coupling reactions. Suitable for researchers and industrial applications, this product is available in >98% purity (GC) with rigorous QC testing to ensure consistency. Store under inert conditions to maintain stability.

CAS No: 123950-44-7
Molecular Formula: C7H4F5N
Molecular Weight: 197.10
Exact Mass: 197.02638994
Monoisotopic Mass: 197.02638994
IUPAC Name: 3,5-difluoro-4-(trifluoromethyl)aniline
SMILES: C1=C(C=C(C(=C1F)C(F)(F)F)F)N
Synonyms: 4-Amino-2,6-difluorobenzotrifluoride, 640-311-4, 123950-44-7, 3,5-difluoro-4-(trifluoromethyl)aniline, Benzenamine, 3,5-difluoro-4-(trifluoromethyl)-

Application

4-Amino-2,6-difluorobenzotrifluoride is widely used as a key intermediate in the synthesis of active pharmaceutical ingredients (APIs) and specialty chemicals. Its electron-deficient aromatic ring facilitates reactions like Buchwald-Hartwig amination or Suzuki-Miyaura coupling. The compound is also employed in agrochemical research to develop herbicides and pesticides with enhanced efficacy. Additionally, it serves as a precursor for fluorinated liquid crystals and polymers in material science.

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