14598-91-5

Basic information

• Product Name: 2-Benzyloxycarbonylamino-3-thiazol-4-yl-propionic acid
• CAS NO: 14598-91-5
• Molecular Weight: 306.342
• Mol File: 14598-91-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-Benzyloxycarbonylamino-3-thiazol-4-yl-propionic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Benzyloxycarbonylamino-3-thiazol-4-yl-propionic acid(14598-91-5)
• EPA Substance Registry System: 2-Benzyloxycarbonylamino-3-thiazol-4-yl-propionic acid(14598-91-5)

Safety Data

• Hazardous Substances Data: 14598-91-5(Hazardous Substances Data)

Upstream product

• 14717-97-6 2-Amino-3-(4-thiazolyl)-propanoic acid 
• 501-53-1 benzyl chloroformate 
• 127862-85-5 2-Benzyloxycarbonylamino-3-thiazol-4-yl-propionic acid 2,2,2-trifluoro-ethyl ester 
• 501-53-1 carbonochloridic acid benzyl ester 

Downstream Products

• 14717-98-7 N-(2-benzyloxycarbonylamino-3-thiazol-4-yl-propionyl)-glycine benzyl ester 
• 127862-85-5 2-Benzyloxycarbonylamino-3-thiazol-4-yl-propionic acid 2,2,2-trifluoro-ethyl ester 
• 14598-94-8 N-(2-benzyloxycarbonylamino-3-thiazol-4-yl-propionyl)-glycine 
• 14598-93-7 N'-(2-benzyloxycarbonylamino-3-thiazol-4-yl-propionyl)-hydrazinecarboxylic acid tert-butyl ester 
• 14598-92-6 2-benzyloxycarbonylamino-3-thiazol-4-yl-propionic acid 4-nitro-phenyl ester 

Relevant articles and documents

Resolution of non-proteinogenic amino acids via microbial lipase-catalyzed enantioselective transesterification

A number of non-proteinogenic amino acids bearing aliphatic side chains were resolved with moderate to good enantioselectivities (E = 15-42) through the Burkholderia cepacia lipase-catalyzed enantioselective transesterification of the 2,2,2-trifluoroethyl esters of their N-benzyloxycarbonyl derivatives with methanol as a nucleophile in diisopropyl ether.

Studies of unnatural amino acids and their peptides. II. The syntheses of DL-beta-(4-thiazolyl)-alpha-alanine and its peptides.

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