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Benzenepropanoic acid, b-[2-(methylamino)-2-oxoethyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92410-30-5

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92410-30-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92410-30-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,4,1 and 0 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 92410-30:
(7*9)+(6*2)+(5*4)+(4*1)+(3*0)+(2*3)+(1*0)=105
105 % 10 = 5
So 92410-30-5 is a valid CAS Registry Number.

92410-30-5SDS

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 5-N-Methyl-3-phenylglutaramic acid

1.2 Other means of identification

Product number -
Other names 4-(N-methylcarbamoyl)-3-phenylbutyric acid

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:92410-30-5 SDS

92410-30-5Relevant academic research and scientific papers

SPIRO-SUBSTITUTED AZACYCLES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY

-

, (2008/06/13)

The present invention is directed to spiro-substituted azacycles of the Formula 1: STR1 (wherein R 1, l, m, Q, W, X, Y, and Z are defined herein) which are useful as modulators of chemokine receptor activity. In particular, these compounds are useful as modulators of the chemokine receptors CCR-1, CCR-2, CCR-2A, CCR-2B, CCR-3, CCR-4, CCR-5, CXCR-3, and/or CXCR-4.

Possible Antineoplastic Agents: Part VIII - Synthesis and Antineoplastic Activity of 5-N-Substituted 3-p-Substituted-phenylglutaramic Acids and 5-N-Substituted 2-Benzenesulphonyl-3-phenyl-L-glutamines

De, A. U.,Mazumdar, Anjali,Jha, Tarun,Debnath, Asim Kumar

, p. 97 - 98 (2007/10/02)

A few 5-N-substituted 3-p-substituted-phenylglutaramic acids (II) and 5-N-substituted 2-benzenesulphonyl-3-phenyl-L-glutamines (V) have been synthesized as structural variants of glutamic acid and evaluated for their activity against Ehrlich ascites carcinoma (EAC) in Swiss albino mice.Quantitative structure activity relationship (QSAR) has been determined employing de novo model to the compounds.The glutaramic acids (II) exhibit better correlation and antineoplastic activity than the glutamines (V).

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