39748-15-7

Basic information

• Product Name: methyl 2-isocyanopropanoate
• CAS NO: 39748-15-7
• Molecular Weight: 113.116
• Mol File: 39748-15-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: methyl 2-isocyanopropanoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2-isocyanopropanoate(39748-15-7)
• EPA Substance Registry System: methyl 2-isocyanopropanoate(39748-15-7)

Safety Data

• Hazardous Substances Data: 39748-15-7(Hazardous Substances Data)

Upstream product

• 799779-64-9 methyl (2S)-2-isocyanopropanoate 
• 32221-83-3 (S)-N-formylalanine methyl ester 
• 44804-83-3 N-formyl-D,L-alanine methyl ester 

Downstream Products

• 117176-06-4 (S)-4-Methyl-4,5-dihydro-oxazole-4-carboxylic acid methyl ester 
• 125294-76-0 (Z)-2-Isocyano-2,3-dimethyl-5-phenyl-5-trimethylsilanyloxy-pent-4-enoic acid methyl ester 
• 65484-40-4 2-Isocyan-N-<(S)-1'-phenylethyl>propionsaeureamid 
• 1040528-99-1 2-isocyano-2-methyl-3-(4-(4,4,5,5-tetramethyl(1,3,2)dioxaborolan-2-yl)-phenyl)-propionic acid methyl ester 
• 74531-02-5 1-Benzyl-4-methyl-2-oxoimidazolidin-4-carbonsaeure-methylester 
• 125294-60-2 2-Isocyano-2-(3-oxo-cyclohexyl)-propionic acid methyl ester 
• 125294-68-0 Methyl 2-isocyano-2-<3-(trimethylsilyloxy)cyclohex-2-enyl>propionate 
• 54011-35-7 Methyl-α-(3.4.5-trimethoxybenzoyl)alaninmethylester 
• 120133-99-5 cis-4-(methoxycarbonyl)-4-methyl-5-methyl-2-oxazoline 
• 120133-99-5 trans-4-(methoxycarbonyl)-4-methyl-5-methyl-2-oxazoline 
• 120133-99-5 (4S,5R)-4-(methoxycarbonyl)-4-methyl-5-methyl-2-oxazoline 
• 120133-99-5 (4R,5S)-4-(methoxycarbonyl)-4-methyl-5-methyl-2-oxazoline 
• 63348-62-9 N-Benzyl-2-isocyanpropionsaeureamid 
• 120133-93-9 (4S,5R)-4-(methoxycarbonyl)-4-methyl-5-phenyl-2-oxazoline 

Relevant articles and documents

Chiral trans-carboxylic trifluoromethyl 2-imidazolines by a Ag2O-catalyzed Mannich-type reaction

Trifluoromethyl aldimines derived from α-amino esters have proven to be very good starting materials to obtain the title compounds. A Ag2O-catalyzed Mannich-type/cyclization cascade reaction starting from suitable α-isocyano acetates leads to e

Investigation of the configurational stabilities of chiral isocyanoacetates in multicomponent reactions

Isocyanoacetates are uniquely reactive compounds characterized by an ambivalent isocyano functional group and an enolizable α-carbon. It is widely believed that chiral α-substituted isocyanoacetates are configurationally unstable in some synthetically use