107479-82-3

Basic information

• Product Name: styrylcarbamic acid ethyl ester
• Synonyms: styrylcarbamic acid ethyl ester
• CAS NO: 107479-82-3
• Molecular Weight: 191.23
• Mol File: 107479-82-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: styrylcarbamic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: styrylcarbamic acid ethyl ester(107479-82-3)
• EPA Substance Registry System: styrylcarbamic acid ethyl ester(107479-82-3)

Safety Data

• Hazardous Substances Data: 107479-82-3(Hazardous Substances Data)

Upstream product

• 64-17-5 ethanol 
• 4737-20-6 cinnamoyl isocyanate 
• 328012-09-5 (E)-1-(1H-benzo[d][1,2,3]triazol-1-yl)-3-phenylprop-2-en-1-one 
• 588-72-7 [(E)-2-bromoethenyl]benzene 
• 7028-48-0 Phenylacetaldehyde oxime 
• 541-41-3 chloroformic acid ethyl ester 
• 33066-20-5 (E)-1-isocyanato-2-phenylethene 

Downstream Products

• 6970-83-8 ethyl-N-(2-phenethyl)carbamate 
• 7664-41-7 ammonia 
• 122-78-1 phenylacetaldehyde 

Relevant articles and documents

An efficient one-pot synthesis of: N, N ′-disubstituted ureas and carbamates from N -acylbenzotriazoles

A facile and high-yielding one-pot synthesis of carbamates and N,N′-disubstituted symmetrical ureas from N-acylbenzotriazoles has been devised. It is believed that, the intermediate acyl-azide undergo Curtius rearrangement and in different solvents gives different products i.e. carbamates in alcohols and N,N′-disubstituted symmetrical urea in THF.

Regioselective cationic reduction of 2-aryl-1-N-(ethoxycarbonyl)enamines to 2-arylethylamine carbamates

2-Aryl-1-N-carboalkoxyenamines (enamides) are selectively reduced to the corresponding 2-arylethylamine carbamates by Et3SiH in the presence of CF3COOH in excellent yields. The reduction proceeds by addition of hydride at C-1 and the

Process for the synthesis of isocyanates and of isocyanate derivatives

The present invention relates to a process for the synthesis of isocyanates and of isocyanate derivatives. Isocyanates are obtained by reacting an organic halide with a metal cyanate in an organic medium in the presence of a catalyst consisting of a complex of nickel with at least one organic ligand, in which complex the nickel is in the zero oxidation state. A carbamate or a urea, respectively, are obtained by a subsequent reaction with a hydroxy compound or a primary or secondary amine. Isocyanates and their derivatives are used especially either as refined synthesis agents for the production of pesticides and medications, or as monomers or comonomers for the preparation of many macromolecular compounds.