106578-69-2

Basic information

• Product Name: 3-Buten-2-one, 1,1,1-trifluoro-4-phenyl-4-(phenylamino)-, (3Z)-
• Synonyms: 4-Anilino-4-phenyl-1,1,1-trifluor-3-buten-2-on
• CAS NO: 106578-69-2
• Molecular Formula: C16H12F3NO
• Molecular Weight: 291.273
• Mol File: 106578-69-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-Buten-2-one, 1,1,1-trifluoro-4-phenyl-4-(phenylamino)-, (3Z)-(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Buten-2-one, 1,1,1-trifluoro-4-phenyl-4-(phenylamino)-, (3Z)-(106578-69-2)
• EPA Substance Registry System: 3-Buten-2-one, 1,1,1-trifluoro-4-phenyl-4-(phenylamino)-, (3Z)-(106578-69-2)

Safety Data

• Hazardous Substances Data: 106578-69-2(Hazardous Substances Data)

Upstream product

• 106578-67-0 (Z)-1,1,1-Trifluoro-4-methylamino-4-phenyl-but-3-en-2-one 
• 106578-65-8 (Z)-4-Amino-1,1,1-trifluoro-4-phenyl-but-3-en-2-one 
• 144864-93-7 1-phenyl-4,4,4-trifluorobutane-1,3-dione 
• 62-53-3 aniline 
• 75840-25-4 (Z)-3-amino-4,4,4-trifluoro-1-phenylbut-2-en-1-one 
• 106578-75-0 1-phenyl-3-(N-methylamino)-4,4,4-trifluoro-2-buten-1-one 

Downstream Products

• 106578-67-0 (Z)-1,1,1-Trifluoro-4-methylamino-4-phenyl-but-3-en-2-one 
• 95332-44-8 4-phenyl-1,1,1-trifluoro-4-(N-phenylamino)-3-butene-2-thione 
• 1524-15-8 4,4,4-trifluoro-3-hydroxy-1-phenylbutan-1-one 
• 80768-54-3 (+/-)-E-1,1,1-trifluoro-4-phenylbut-3-en-2-ol 
• 130240-26-5 1-phenyl-4,4,4-trifluoro-1,2-butanediol 

Relevant articles and documents

Interaction of fluoroalkyl-containing β-diketones with amines

The composition of products of the interaction of asymmetric fluoroalkyl-containing β-diketones with amines was studied. Mixtures of regioisomeric β-aminovinylketones and products of cleavage and secondary condensation are formed, depending on the temperature, the solvent, the nature of the fluorinated and nonfluorinated substituents in the β-diketone, and the basicity of the amine. The major product is a β-aminovinylketone in which the NH2 group is removed from the fluoroalkyl substituent. No β-aminovinylimines, products of condensation involving two electrophilic centers, were observed.

Reactions of α-alkyl- and α-aryl-substituted N-benzylideneamines with trihaloacetylating agents

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