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1H-Pyrazole-3-propanoic acid, 5-(4-bromophenyl)-a-(3-methylphenyl)-1-(4-methylphenyl)-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

648869-40-3

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648869-40-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 648869-40-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,8,8,6 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 648869-40:
(8*6)+(7*4)+(6*8)+(5*8)+(4*6)+(3*9)+(2*4)+(1*0)=223
223 % 10 = 3
So 648869-40-3 is a valid CAS Registry Number.

648869-40-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[5-(4-bromo-phenyl)-1-p-tolyl-1H-pyrazol-3-yl]-2-m-tolyl-propionic acid ethyl ester

1.2 Other means of identification

Product number -
Other names 3-[5-(4-bromophenyl)-1-p-tolyl-1H-pyrazol-3-yl]-2-m-tolylpropionic acid ethyl ester

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:648869-40-3 SDS

648869-40-3Relevant academic research and scientific papers

Alpha,beta-unsaturated esters and acids by stereoselective dehydration

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Page/Page column 83, (2010/02/15)

There are provided by the present invention certain pyrazole based CCK-1 receptor modulators which have the general formula: wherein Ar is an aromatic or heteroaromatic group, X is a hydrocarbon linker, Y is a bond or hydrocarbon linker and R1, R2, R3, R4 and R5 are certain organic substituents, methods for making the same, and stereoselective dehydration methods for generally making α,β-unsaturated esters, acids and their derivatives.

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