2768-50-5

Basic information

• Product Name: H-GLU(OBZL)-OBZL
• Synonyms: H-GLU(OBZL)-OBZL;L-Glutamic acid, bis(phenylmethyl) ester
• CAS NO: 2768-50-5
• Molecular Formula: C₁₉H₂₁NO₄
• Molecular Weight: 327.37434
• Mol File: 2768-50-5.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: H-GLU(OBZL)-OBZL(CAS DataBase Reference)
• NIST Chemistry Reference: H-GLU(OBZL)-OBZL(2768-50-5)
• EPA Substance Registry System: H-GLU(OBZL)-OBZL(2768-50-5)

Safety Data

• Hazardous Substances Data: 2768-50-5(Hazardous Substances Data)

Upstream product

• 56-86-0 L-glutamic acid 
• 98-11-3 benzenesulfonic acid 
• 100-51-6 benzyl alcohol 
• 6192-52-5 p-toluenesulfonic acid monohydrate 
• 1155-62-0 N-benzyloxycarbonyl-L-glutamic acid 
• 80963-14-0 dibenzyl N-tert-butyloxycarbonyl-L-glutamate 
• 4561-10-8 L-glutamic acid dibenzyl ester hydrochloride 
• 130289-55-3 dibenzyl ester of L-glutamic acid p-toluenesulfonate 
• 103156-77-0 Cbz-L-Glu(OBzl)-OBzl 

Downstream Products

• 31059-79-7 (S)-2-[(S)-2-Benzyloxycarbonylamino-4-(4-nitro-phenoxycarbonyl)-butyrylamino]-pentanedioic acid dibenzyl ester 
• 6163-75-3 dimethyl ethylphosphonate 
• 59524-71-9 t-butoxycarbonyl-L-alanyl-L-glutamic acid dibenzyl ester 
• 200941-07-7 C₂₇H₃₀NO₆P 
• 200941-05-5 N-[benzyloxy(phenyl)phosphinyl]-L-glutamic acid dibenzyl ester 
• 870822-44-9 N-{benzyloxy[2-(4-methoxyphenyl)ethyl]phosphinyl}-L-glutamic acid dibenzyl ester 
• 870822-43-8 N-{benzyloxy[2-(4-methylphenyl)ethyl]phosphinyl}-L-glutamic acid dibenzyl ester 
• 870822-45-0 N-{benzyloxy[2-(4-cyclohexylphenyl)ethyl]phosphinyl}-L-glutamic acid dibenzyl ester 
• 1116-22-9 γ-L-glutamyl-L-glutamic acid 
• 1116-22-9 (R)-2-((S)-4-amino-4-carboxybutanamido)pentanedioic acid 
• 3705-42-8 Cbz-(L)-Glu-OBn 
• 7365-90-4 benzyloxycarbonyl-α-benzyl-γ-L-glutamyl-D-glutamic acid dibenzyl ester 
• 7365-90-4 benzyloxycarbonyl-α-benzyl-γ-L-glutamyl-L-glutamic acid dibenzyl ester 
• 97154-87-5 N-(O-benzyl-N-benzyloxycarbonyl-L-γ-glutamyl)-D-alanine benzyl ester 

Relevant articles and documents

A class of novel conjugates of substituted purine and Gly-AA-OBzl: Synthesis and evaluation of orally analgesic activity

Aimed at the chemotherapy of chronic pain two kinds of analgesic pharmacophores, substituted purine and Gly-AA-OBzl, were coupled via a five-step-reaction procedure and 19 novel conjugates N-[2-chloro-9- (tetrahydropyran-2-yl)-9H-purin-6-yl]-N-cyclopropylglycylamino acid benzylesters were provided. On mouse-tail flick model their in vivo analgesic activities were assayed. The results indicate that introducing Gly-OC2H 5 into the 6-position of the substituted purine leads to ambiguous increase of the analgesic activity, while introducing Gly-AA-OBzl into this position leads to significant increase of the analgesic activity.

A torsional strain mechanism to tune pitch in supramolecular helices

(Figure Presented) On the turn: Torsional strain has been used to control the pitch of helical nanostructures in the range of tens to hundreds of nanometers. In this method, sterically induced torsional strain on the primary helices forces the secondary h