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"Benzyloxycarbonyl-γ-benzyl-α-L-glutamyl-L-glutamic acid dibenzyl ester" is a complex organic compound with the molecular formula C41H42N2O8. It is a peptide derivative, characterized by the presence of a benzyloxycarbonyl (Cbz) protecting group, a γ-benzyl group, and two glutamic acid residues connected through their α-carboxylic acid groups. The dibenzyl ester indicates that both carboxylic acid groups of the glutamic acid residues are esterified with benzyl groups. benzyloxycarbonyl-γ-benzyl-α-L-glutamyl-L-glutamic acid dibenzyl ester is often used in peptide synthesis as a protected intermediate, where the protecting groups can be selectively removed to yield the desired peptide sequence. The benzyl groups are typically removed using catalytic hydrogenation or other deprotection methods, allowing for the controlled assembly of larger peptide structures.

6922-66-3

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6922-66-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6922-66-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,2 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6922-66:
(6*6)+(5*9)+(4*2)+(3*2)+(2*6)+(1*6)=113
113 % 10 = 3
So 6922-66-3 is a valid CAS Registry Number.

6922-66-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyloxycarbonyl-γ-benzyl-α-L-glutamyl-L-glutamic acid dibenzyl ester

1.2 Other means of identification

Product number -
Other names N-(O-Benzyl-N-benzyloxycarbonyl-L-α-glutamyl)-L-glutaminsaeure-dibenzylester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6922-66-3 SDS

6922-66-3Downstream Products

6922-66-3Relevant academic research and scientific papers

Synthesis of γ-Glutamyl Peptides Catalyzed by Transamidase from Bacillus natto

Noda, Kosaku,Igata, Keiko,Horikawa, Yoshiko,Fujii, Hisao

, p. 2419 - 2424 (2007/10/02)

Crude ammonium sulfate fraction of a cell free extract from Bacillus natto contained an enzyme (or enzymes) which catalyzed the transamidation reaction specific for glutamine.Both L- and D-isomers of glutamine were active as substrate.On incubation of L- or D-glutamine with the enzyme preparation, two peptides consisting of glutamic acid and glutamine were formed.The main component of the peptides was readily isolated by ion-exchange chromatography and identified as γ-glutamylglutamine by paper chromatography and by paper electrophoresis using authentic peptides.The optical configuration of the amino acid residues in the dipeptide was determined by digestion of the acid hydrolyzate with L-glutamic acid decarboxylase, and the result showed that the dipeptide obtained from L-glutamine was a L-L isomer, while the dipeptide from D-glutamine was a D-D isomer.

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