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209127-97-9

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209127-97-9 Usage

General Description

The chemical compound [(RS)-2-carboxy-3-phenylpropionyl]-Leu-OH is a synthetic peptide derivative with the molecular formula C21H25NO4. It is a modified form of the amino acid leucine, with an additional carboxy-phenylpropionyl group attached to the amine group of the leucine side chain. This modification alters the chemical and biological properties of the peptide, potentially affecting its solubility, stability, and receptor binding affinity. The compound may have applications in biochemical and pharmaceutical research, particularly in the study of peptide structure-activity relationships and the development of novel peptide-based therapeutics.

Check Digit Verification of cas no

The CAS Registry Mumber 209127-97-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,9,1,2 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 209127-97:
(8*2)+(7*0)+(6*9)+(5*1)+(4*2)+(3*7)+(2*9)+(1*7)=129
129 % 10 = 9
So 209127-97-9 is a valid CAS Registry Number.

209127-97-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-Carboxy-3-phenylpropanoyl)-L-leucine

1.2 Other means of identification

Product number -
Other names (R)-N-(methoxymethyl)-1-phenyl-N-((trimethylsilyl)methyl)ethanamine

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:209127-97-9 SDS

209127-97-9Downstream Products

209127-97-9Relevant articles and documents

New carboxyalkyl inhibitors of brain enkephalinase: Synthesis, biological activity, and analgesic properties

Fournie Zaluski,Chaillet,Soroca Lucas,Fournie-Zaluski,Marcais-Collado,Costentin,Roques

, p. 60 - 65 (2007/10/02)

New carboxylalkyl compounds derived from Phe-Leu and Phe-Ala were synthesized and checked as inhibitors of enkephalinase, a metalloendopeptidase cleaving the Gly3-Phe4 bond of enkephalins from mouse striatal membranes. Differential r

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