121145-33-3

Basic information

• Product Name: (S)-1-(3,6-Dihydro-2H-pyridin-1-yl)-3,3,3-trifluoro-2-methoxy-2-phenyl-propan-1-one
• Synonyms: (S)-1-(3,6-Dihydro-2H-pyridin-1-yl)-3,3,3-trifluoro-2-methoxy-2-phenyl-propan-1-one
• CAS NO: 121145-33-3
• Molecular Weight: 299.293
• Mol File: 121145-33-3.mol

Chemical Properties

• CAS DataBase Reference: (S)-1-(3,6-Dihydro-2H-pyridin-1-yl)-3,3,3-trifluoro-2-methoxy-2-phenyl-propan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-1-(3,6-Dihydro-2H-pyridin-1-yl)-3,3,3-trifluoro-2-methoxy-2-phenyl-propan-1-one(121145-33-3)
• EPA Substance Registry System: (S)-1-(3,6-Dihydro-2H-pyridin-1-yl)-3,3,3-trifluoro-2-methoxy-2-phenyl-propan-1-one(121145-33-3)

Safety Data

• Hazardous Substances Data: 121145-33-3(Hazardous Substances Data)

Upstream product

• 694-05-3 1,2,3,6-tetrahydropyridine 
• 17257-71-5 (S)-Mosher acid 

Downstream Products

• 111612-22-7 (1R)-1-Phenyl-2<(2R)-2-piperidyl>ethanol 
• 121139-20-6 (S)-3,3,3-Trifluoro-2-methoxy-1-[(R)-2-(2-oxo-2-phenyl-ethyl)-piperidin-1-yl]-2-phenyl-propan-1-one 
• 121139-16-0 (S)-1-(3,4-Dihydro-2H-pyridin-1-yl)-3,3,3-trifluoro-2-methoxy-2-phenyl-propan-1-one 

Relevant articles and documents

ASYMMETRIC ELECTROPHILIC α-AMIDOALKYLATION 5: IMPROVED STEREOSELECTIVITIES THROUGH NEW CHIRAL AUXILIARIES

Enamides of type 2 were employed in asymmetric α-amidoalkylation reactions with silyl enol ether 4 as nucleophile.Depending on the chiral auxiliary used, (R)-5/(S)-5 stereoselectivities up to 95/5 could be reached.Based on the obtained results a model for