157042-75-6

Basic information

• Product Name: (4S,5R)-5-(2,6-difluorophenyl)-2-oxazoline-4-(N,N-dimethyl)carboxamide
• CAS NO: 157042-75-6
• Molecular Weight: 254.236
• Mol File: 157042-75-6.mol

Chemical Properties

• CAS DataBase Reference: (4S,5R)-5-(2,6-difluorophenyl)-2-oxazoline-4-(N,N-dimethyl)carboxamide(CAS DataBase Reference)
• NIST Chemistry Reference: (4S,5R)-5-(2,6-difluorophenyl)-2-oxazoline-4-(N,N-dimethyl)carboxamide(157042-75-6)
• EPA Substance Registry System: (4S,5R)-5-(2,6-difluorophenyl)-2-oxazoline-4-(N,N-dimethyl)carboxamide(157042-75-6)

Safety Data

• Hazardous Substances Data: 157042-75-6(Hazardous Substances Data)

Upstream product

• 437-81-0 2,6-difluorobenzaldehyde 
• 68157-98-2 N,N-dimethyl-α-isocyanoacetamide 

Relevant articles and documents

Gold(I)-catalyzed asymmetric aldol reactions of isocyanoacetic acid derivatives with fluoroaryl aldehydes

The catalytic asymmetric synthesis of stereochemically defined fluoro-phenylserines is reported. In the title reaction, when methyl isocyanoacetate is employed, the number of fluorine atoms in the phenyl ring of benzaldehyde controls stereochemical outcom

Gold(I)-catalyzed asymmetric aldol reactions of fluorinated benzaldehydes with an α-isocyanoacetamide

The use of N,N-dimethyl-α-isocyanoacetamide instead of methyl α-isocyanoacetate in the gold(I)-catalyzed asymmetric aldol reactions with polyfluorinated benzaldehydes was found to improve both diastereo- and enantioselectivity in the formation of trans-ox