1190882-06-4

Basic information

• Product Name: (2S)-2-(N-allyl-N-((S)-1-phenylethyl)amino)-2-(4-fluorophenyl)-N-methylacetamide
• CAS NO: 1190882-06-4
• Molecular Weight: 326.414
• Mol File: 1190882-06-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2S)-2-(N-allyl-N-((S)-1-phenylethyl)amino)-2-(4-fluorophenyl)-N-methylacetamide(CAS DataBase Reference)
• NIST Chemistry Reference: (2S)-2-(N-allyl-N-((S)-1-phenylethyl)amino)-2-(4-fluorophenyl)-N-methylacetamide(1190882-06-4)
• EPA Substance Registry System: (2S)-2-(N-allyl-N-((S)-1-phenylethyl)amino)-2-(4-fluorophenyl)-N-methylacetamide(1190882-06-4)

Safety Data

• Hazardous Substances Data: 1190882-06-4(Hazardous Substances Data)

Upstream product

• 1021452-36-7 2-(N-allyl-N-((S)-1-phenylethyl)amino)-N-tert-butoxy-N-methylacetamide 
• 133472-27-2 4-fluorophenylzinc chloride 

Relevant articles and documents

Synthesis of α-amino amides via N,O-acetals derived from Weinreb amides

(Chemical Equation Presented) An easy and straightforward synthesis of α-amino amides via a base-mediated rearrangement of modified Weinreb amides into N,O-acetals is presented. Subsequent arylation, alkylation, alkenylation, or alkynylation of this intermediate affords the corresponding R-amino amides in excellent yields. Furthermore, a more generalized protocol for the α-arylation of Weinreb amides lacking an R-amino moiety is also discussed.