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

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

• 103156-77-0 Cbz-L-Glu(OBzl)-OBzl 
• 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 

Downstream Products

• 96675-47-7 N-(N-benzyloxycarbonyl-L-γ-glutamyl)-L-glutamic acid dibenzyl ester 
• 122702-26-5 N-(N²-benzyloxycarbonyl-N⁵-carbamoyl-L-ornithyl)-L-glutamic acid dibenzyl ester 
• 79220-31-8 N-(N^α,N^δ,N^ω-tris-benzyloxycarbonyl-L-arginyl)-L-glutamic acid dibenzyl ester 
• 13030-09-6 1-benzyl L-glutamate 
• 2601-49-2 N-Benzyloxycarbonyl-S-benzyl-L-cysteinyl-L-glutaminsaeure-dibenzylester 
• 4159-71-1 Phenylalanyl-glutaminsaeure 
• 1676-73-9 L-glutamic acid γ-benzyl ester 
• 128135-40-0 (2S)-(3-carboxypropionylamino)pentanedioic acid dibenzyl ester 
• 5276-60-8 N-(N-benzyloxycarbonyl-L-alanyl)-L-glutamic acid dibenzyl ester 
• 3062-06-4 Benzyloxycarbonyl-L-valyl-L-glutaminsaeure-dibenzylester 
• 89092-61-5 N-tertbutyloxycarbonyl dipeptide of benzyl glutamate 
• 130289-56-4 N-(α,α-diphenyl-α-chloroacetyl)glutamic dibenzylate 
• 120612-70-6 Z2>Arg-Glu(OBzl)2 
• 149836-41-9 Boc-Val-Glu(OBzl)-OBzl 

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.

Study on synthesis, characteristics and catalysis properties of novel chiral metal complexes catalysts for 1,3-dipolar cycloaddition reactions of nitrone with electron-rich alkene

As a new class of potential catalysts for 1,3-dipolar cycloaddition reactions, fourteen L-amino acid Schiff base Cu(II) and Ti(IV) complexes were synthesized, characterized, and evaluated for their catalytic activities in the reaction between C, N-diphenylnitrone and electron-rich ethyl vinyl ether under both homogeneous and in situ conditions. The methods for preparation and utilization of the catalysts were elucidated in detail, and the results of the catalytic reactions were described and discussed as well. Excellent reaction results were found in the presence of some catalysts (20 mol%) with > 90% endo-isoazolidines produced, compared with predominantly exo-isoazolidine produced without a catalyst. In addition, the reaction rate is found to be enhanced remarkably by a Cu(II) complex Schiff base catalyst at room temperature.

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