95332-44-8

Basic information

• Product Name: 4-phenyl-1,1,1-trifluoro-4-(N-phenylamino)-3-butene-2-thione
• Synonyms: 4-phenyl-1,1,1-trifluoro-4-(N-phenylamino)-3-butene-2-thione
• CAS NO: 95332-44-8
• Molecular Weight: 307.339
• Mol File: 95332-44-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 4-phenyl-1,1,1-trifluoro-4-(N-phenylamino)-3-butene-2-thione(CAS DataBase Reference)
• NIST Chemistry Reference: 4-phenyl-1,1,1-trifluoro-4-(N-phenylamino)-3-butene-2-thione(95332-44-8)
• EPA Substance Registry System: 4-phenyl-1,1,1-trifluoro-4-(N-phenylamino)-3-butene-2-thione(95332-44-8)

Safety Data

• Hazardous Substances Data: 95332-44-8(Hazardous Substances Data)

Upstream product

• 106578-69-2 1-phenyl-1-(N-phenylamino)-4,4,4-trifluoro-1-buten-3-one 
• 100890-80-0 4-phenyl-1,1,1-trifluoro-4-amino-3-butene-2-thione 
• 62-53-3 aniline 
• 108959-54-2 1-phenyl-4,4,4-trifluoro-3-mercapto-2-buten-1-one 

Downstream Products

• 100890-80-0 4-phenyl-1,1,1-trifluoro-4-amino-3-butene-2-thione 

Relevant articles and documents

THE REACTIONS OF AMINO AND THIO DERIVATIVES OF POLYFLUORINATED β-DIKETONES WITH AMINES

A study was carried out on the aminolysis of isomeric polyfluorinated β-aminovinylthiones and monothio-β-diketones with geminal fluoroalkyl and mercapto groups. β-Aminovinylthiones react with amines at the enamine electrophilic site, while monothio-β-diketones react at the electrophilic site attached to the nonfluorinated substituent.Intrachelate prototropic tautomerism is presumably one of the factors responsible for the reaction regiospecificity.