106189-00-8

Basic information

• Product Name: Phenylalanine, b-hydroxy-N-[N-[(phenylmethoxy)carbonyl]glycyl]-
• CAS NO: 106189-00-8
• Molecular Formula: C19H20N2O6
• Molecular Weight: 372.378
• Mol File: 106189-00-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Phenylalanine, b-hydroxy-N-[N-[(phenylmethoxy)carbonyl]glycyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenylalanine, b-hydroxy-N-[N-[(phenylmethoxy)carbonyl]glycyl]-(106189-00-8)
• EPA Substance Registry System: Phenylalanine, b-hydroxy-N-[N-[(phenylmethoxy)carbonyl]glycyl]-(106189-00-8)

Safety Data

• Hazardous Substances Data: 106189-00-8(Hazardous Substances Data)

Upstream product

• 15917-28-9 (2RS,3SR)-2-amino-3-hydroxy-3-phenyl-propionic acid ethyl ester 
• 69-96-5 dl-threo-phenylserine 
• 80182-99-6 β-hydroxyphenylalanine methyl ester hydrochloride 
• 1138-80-3 N-(Benzyloxycarbonyl)glycine 
• 42267-16-3 (d,l)-phenylserine ethyl ester hydrochloride 
• 106111-12-0 Z-Gly-PhSer-OMe 

Downstream Products

• 69181-24-4 (4-benzylidene-5-oxo-4,5-dihydro-oxazol-2-ylmethyl)-carbamic acid benzyl ester 
• 106189-01-9 N-benzyloxycarbonyl-glycyl-(Z)-dehydrophenylalanyl(S)leucine methyl ester 
• 145763-46-8 (S)-2-{(S)-2-[2-(2-{(S)-2-Benzyloxycarbonylamino-3-[4-(toluene-4-sulfonyloxy)-phenyl]-propionylamino}-acetylamino)-acetylamino]-3-phenyl-propionylamino}-4-methyl-pentanoic acid methyl ester 
• 145763-47-9 (S)-2-{(R)-2-[2-(2-{(S)-2-Benzyloxycarbonylamino-3-[4-(toluene-4-sulfonyloxy)-phenyl]-propionylamino}-acetylamino)-acetylamino]-3-phenyl-propionylamino}-4-methyl-pentanoic acid methyl ester 
• 106111-08-4 N-benzyloxycarbonyl-O-tosyl-(S)tyrosyl-glycyl-glycyl-(Z)dehydrophenylalanyl-(S)leucine methyl ester 
• 761366-27-2 (S)-H-Gly-ΔPhe-Leu-OMe 

Relevant articles and documents

SYNTHESIS OF A PROTECTED MONODEHYDRO Leu-ENKEPHALIN AND ITS HYDROGENATION CATALYZED BY CHIRAL RHODIUM COMPLEXES

(S,S)-Z-(O)Ts-Tyr-Gly2-ΔPhe-Leu-OMe was synthesized.Some chiral rhodium complexes catalyze the reduction of the C=C bond.The stereochemistry of reduction of the ΔPhe moiety was investigated. 93 percent de could be achieved with dipamp as ligand in the cat