1177023-45-8

Basic information

• Product Name: (E)-3-morpholino-1-[4-(trifluoromethyl)phenyl]prop-2-en-1-one
• Synonyms: (E)-3-morpholino-1-[4-(trifluoromethyl)phenyl]prop-2-en-1-one
• CAS NO: 1177023-45-8
• Molecular Weight: 285.266
• Mol File: 1177023-45-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (E)-3-morpholino-1-[4-(trifluoromethyl)phenyl]prop-2-en-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-3-morpholino-1-[4-(trifluoromethyl)phenyl]prop-2-en-1-one(1177023-45-8)
• EPA Substance Registry System: (E)-3-morpholino-1-[4-(trifluoromethyl)phenyl]prop-2-en-1-one(1177023-45-8)

Safety Data

• Hazardous Substances Data: 1177023-45-8(Hazardous Substances Data)

Upstream product

• 455-19-6 4-Trifluoromethylbenzaldehyde 
• 110-91-8 morpholine 
• 67081-98-5 (+/-)-1-<4-(trifluoromethyl)phenyl>-1-propanol 
• 711-33-1 4-trifluoromethyl propiophenone 
• 121-97-1 4-Methoxypropiophenone 

Downstream Products

• 1323116-56-8 3-morpholino-1-[4-(trifluoromethyl)phenyl]propan-1-ol 

Relevant articles and documents

Transformation of α-substituted propanols into γ-amino alcohols through nickel-catalyzed amination on the terminal γ-carbon of propanols

A nickel-phosphine complex was found to be effective as the catalyst for the transformation of alcohols into β-enaminones, which was successively converted into γ-amino alcohols by a conventional reductant. The sequential transformation is equivalent to the carbon-nitrogen bond formation at the γ-position of saturated alcohols. Georg Thieme Verlag Stuttgart · New York.