890306-83-9

Basic information

• Product Name: (S)-methyl 2-(benzyloxycarbonylamino)-3-(1-methyl-1H-imidazol-4-yl)propanoate
• Synonyms: (S)-methyl 2-(benzyloxycarbonylamino)-3-(1-methyl-1H-imidazol-4-yl)propanoate
• CAS NO: 890306-83-9
• Molecular Weight: 317.345
• Mol File: 890306-83-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (S)-methyl 2-(benzyloxycarbonylamino)-3-(1-methyl-1H-imidazol-4-yl)propanoate(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-methyl 2-(benzyloxycarbonylamino)-3-(1-methyl-1H-imidazol-4-yl)propanoate(890306-83-9)
• EPA Substance Registry System: (S)-methyl 2-(benzyloxycarbonylamino)-3-(1-methyl-1H-imidazol-4-yl)propanoate(890306-83-9)

Safety Data

• Hazardous Substances Data: 890306-83-9(Hazardous Substances Data)

Upstream product

• 71-00-1 L-histidine 
• 4467-54-3 l-histidine methyl ester dihydrochloride 
• 69614-04-6 S-(+)-7-Methoxycarbonyl-5,6,7,8-tetrahydroimidazo<1,5-c>pyrimidin-5-on 
• 69618-95-7 (S)-7-(methoxycarbonyl)-2-methyl-5-oxo-5,6,7,8-tetrahydroimidazo[1,5-c] pyrimidin-2-ium iodide 
• 100-51-6 benzyl alcohol 

Downstream Products

• 1001011-16-0 N-α-(carbobenzyloxy)-N-α-isopropyl,N-1(τ)-methyl-L-histidine methyl ester 
• 1001011-14-8 N-α-(carbobenzyloxy)-N-α-ethyl,N-1(τ)-methyl-L-histidine methyl ester 
• 1001011-15-9 N-α-(carbobenzyloxy)-N-α-propyl,N-1(τ)-methyl-L-histidine methyl ester 
• 1001011-13-7 N-α-(carbobenzyloxy)-N-α,N-1(τ)-dimethyl-L-histidine methyl ester 
• 331-38-4 L-anserine 
• 57519-09-2 (S)-methyl 2-amino-3-(1-methyl-1H-imidazol-4-yl)propanoate 
• 945723-73-9 methanesulfonic acid 2-benzyloxycarbonylamino-3-(1-methyl-1H-imidazol-4-yl)-propyl ester 
• 945723-57-9 3-[1-(methyl)imidazol-4-yl]-(2S)-2-(benzyloxycarbonylamino)propanol 

Relevant articles and documents

Concise Synthesis of Anserine: Efficient Solvent Tuning in Asymmetric Hydrogenation Reaction

A concise synthesis of anserine and related compounds was accomplished by Et-DuPhos-Rh-catalyzed asymmetric hydrogenation of dehydrohistidine derivatives in 2,2,2-trifluoroethanol, which played a key role in improving the yield and selectivity.

Facile regiospecific syntheses of N-α,N-1(τ)-dialkyl-L-histidines

(Chemical Equation Presented) Two diverse methodologies describe the first synthesis of suitably protected N-α,N-1(τ)-dialkyl-L-histidine derivatives. Synthesis of suitably protected N-α,N-1(τ)-dialkyl-L- histidines 7-9 containing different alkyl groups a