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23576-42-3

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23576-42-3 Usage

Definition

ChEBI: A tripeptide composed of one L-phenylalanine and two glycine residues joined in sequence.

Check Digit Verification of cas no

The CAS Registry Mumber 23576-42-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,5,7 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 23576-42:
(7*2)+(6*3)+(5*5)+(4*7)+(3*6)+(2*4)+(1*2)=113
113 % 10 = 3
So 23576-42-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H17N3O4/c14-10(6-9-4-2-1-3-5-9)13(20)16-7-11(17)15-8-12(18)19/h1-5,10H,6-8,14H2,(H,15,17)(H,16,20)(H,18,19)

23576-42-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Phe-Gly-Gly

1.2 Other means of identification

Product number -
Other names phe-gly-gly

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:23576-42-3 SDS

23576-42-3Relevant articles and documents

N -boc deprotection and isolation method for water-soluble zwitterionic compounds

Liu, Zhijian,Yasuda, Nobuyoshi,Simeone, Michael,Reamer, Robert A.

, p. 11792 - 11796 (2015/02/19)

A highly efficient TMSI-mediated deprotection and direct isolation method to obtain zwitterionic compounds from the corresponding N-Boc derivatives has been developed. This method has been demonstrated in the final deprotection/isolation of the β-lactamase inhibitor MK-7655 as a part of its manufacturing process. Further application of this process toward other zwitterionic compounds, such as dipeptides and tripeptides, has been successfully developed. Furthermore, a catalytic version of this transformation has been demonstrated in the presence of BSA or BSTFA.

ATRIOPEPTINS. II. SYNTHESIS OF N-TERMINAL FRAGMENTS

Ovchinnikov, Mikhail V.,Bespalova, Zhanna D.,Molokoedov, Aleksandr S.,Revenko, Inna V.,Sepetov, Nikolai F.,et al

, p. 784 - 795 (2007/10/02)

Peptides, corresponding to the N-terminal sequence in atriopeptins, were synthesized by classical methods of peptide chemistry in solutions.The obtained peptides were characterized by various physicochemical methods.The scheme and methods of the synthesis are discussed.

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