77152-98-8

Basic information

• Product Name: Carbamic acid, (3-amino-3-thioxopropyl)-, phenylmethyl ester
• CAS NO: 77152-98-8
• Molecular Formula: C11H14N2O2S
• Molecular Weight: 238.31
• Mol File: 77152-98-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Carbamic acid, (3-amino-3-thioxopropyl)-, phenylmethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, (3-amino-3-thioxopropyl)-, phenylmethyl ester(77152-98-8)
• EPA Substance Registry System: Carbamic acid, (3-amino-3-thioxopropyl)-, phenylmethyl ester(77152-98-8)

Safety Data

• Hazardous Substances Data: 77152-98-8(Hazardous Substances Data)

Upstream product

• 501-53-1 benzyl chloroformate 
• 18877-96-8 3-<<(benzyloxy)carbonyl>amino>propionitrile 

Downstream Products

• 77153-00-5 S-ethyl-3-<<(benzyloxy)carbonyl>amino>propiothioimidate 
• 92741-55-4 2'-(N-Z-2-aminoethyl)-4-methoxycarbonyl-2,4'-bithiazole 
• 610796-29-7 (R)-3-Benzyloxycarbonylamino-3-[2-(2-benzyloxycarbonylamino-ethyl)-thiazol-4-yl]-propionic acid 
• 92741-56-5 N-<2'-(N''-Z-2-aminoethyl)-2,4'-bithiazole-4-carboxy>-N'-Boc-1,2-diaminoethane 
• 86179-51-3 2'-(2-Carbobenzoxyaminoethyl)-2,4'-bithiazole-4-carboxylic acid 
• 77153-03-8 N-stearoyl-3-<<(benzyloxy)carbonyl>amino>propionamidine 
• 77172-38-4 N-(tert-butoxycarbonyl)-3-<<(benzyloxy)carbonyl>amino>propionamidine 
• 77153-01-6 3-<<(benzyloxy)carbonyl>amino>propionamidine 

Relevant articles and documents

Dithio and thiono esters, LVII: Synthesis of dithio and thiono esters of N-protected β- and γ-amino acids

The N-protected β-aminonitriles 1 were transformed into the imidoester or thiolimidoester hydrochlorides 2 or 3 according to Pinner and sulfhydrolyzed with H2S to give the N-protected β-amino thiono esters 4 or dithio esters 5. Alkylation of th

Acylation of Dibasic Compounds Containing Amino Amidine and Aminoguanidine Functions

The site of acylation in difunctional compounds containing an amine and either an amidine or guanidine can be determined from the ultraviolet absorption spectrum of the acylated product.If the amidine or guanidine has been acylated, the product possesses a chromophore that is pH dependent, whereas if an amide was formed, the chromophore is independent of pH.