735240-08-1

Basic information

• Product Name: 4-(N-benzyl-N-methylamino)butyrophenone
• Synonyms: 4-(N-benzyl-N-methylamino)butyrophenone
• CAS NO: 735240-08-1
• Molecular Weight: 267.371
• Mol File: 735240-08-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 4-(N-benzyl-N-methylamino)butyrophenone(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(N-benzyl-N-methylamino)butyrophenone(735240-08-1)
• EPA Substance Registry System: 4-(N-benzyl-N-methylamino)butyrophenone(735240-08-1)

Safety Data

• Hazardous Substances Data: 735240-08-1(Hazardous Substances Data)

Upstream product

• 103-67-3 benzyl-methyl-amine 
• 939-52-6 4-chloro-1-phenylbutan-1-one 
• 65488-05-3 4-iodobutyrophenone 

Downstream Products

• 947373-08-2 4-(N-benzyl-N-methylamino)-1-phenylbutan-1-ol 

Relevant articles and documents

Efficient asymmetric hydrogenation of β- and γ-amino ketone derivatives leading to practical synthesis of fluoxetine and eprozinol

N-(Methylcarbamoyl)-4-(dicyclohexylphosphino)-2-[(diphenylphosphino)me thyl]pyrrolidine (MCCPM)- and N-(tert-butoxycarbonyl)-4-(dicyclohexylphosphino)-2-[(diphenylphosphin o)methyl]pyrrolidine (BCPM)-rhodium(I) complexes were efficient catalysts for asymmetric hydrogenations of β- and γ-amino ketone hydrochloride derivatives. Utilizing this methodology, we have developed efficient syntheses of fluoxetine and eprozinol from intermediate optically active amino alcohols.