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Atomfair 3,5-Difluoro-4-(trifluoromethyl)phenol C7H3F5O

Description 3,5-Difluoro-4-(trifluoromethyl)phenol (CAS No. 116640-11-0) is a high-purity fluorinated phenolic compound with the molecular formula C7H3F5O . This specialty chemical is characterized by its unique structure featuring two fluorine atoms and a trifluoromethyl group on the aromatic ring, making it a valuable intermediate in advanced organic synthesis and pharmaceutical research. With an IUPAC name of 3,5-difluoro-4-(trifluoromethyl)phenol , this compound is supplied as a crystalline solid with guaranteed purity suitable for demanding applications. Its fluorinated aromatic structure lends itself to use in the development of novel materials, agrochemicals, and bioactive molecules. Proper storage under inert conditions is recommended to maintain stability.

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Description

Description

3,5-Difluoro-4-(trifluoromethyl)phenol (CAS No. 116640-11-0) is a high-purity fluorinated phenolic compound with the molecular formula C7H3F5O. This specialty chemical is characterized by its unique structure featuring two fluorine atoms and a trifluoromethyl group on the aromatic ring, making it a valuable intermediate in advanced organic synthesis and pharmaceutical research. With an IUPAC name of 3,5-difluoro-4-(trifluoromethyl)phenol, this compound is supplied as a crystalline solid with guaranteed purity suitable for demanding applications. Its fluorinated aromatic structure lends itself to use in the development of novel materials, agrochemicals, and bioactive molecules. Proper storage under inert conditions is recommended to maintain stability.

  • CAS No: 116640-11-0
  • Molecular Formula: C7H3F5O
  • Molecular Weight: 198.09
  • Exact Mass: 198.01040553
  • Monoisotopic Mass: 198.01040553
  • IUPAC Name: 3,5-difluoro-4-(trifluoromethyl)phenol
  • SMILES: C1=C(C=C(C(=C1F)C(F)(F)F)F)O
  • Synonyms: 3,5-DIFLUORO-4-(TRIFLUOROMETHYL)PHENOL, 116640-11-0, Phenol, 3,5-difluoro-4-(trifluoromethyl)-, MFCD19441183, SCHEMBL759007

Application

This fluorinated phenol derivative serves as a key building block in pharmaceutical research, particularly in the synthesis of compounds with enhanced metabolic stability. Its electron-withdrawing substituents make it valuable for creating advanced materials with specific electronic properties. Researchers also utilize it in the development of agrochemicals and specialty polymers where fluorine incorporation is desired.

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