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2-Propenamide, N-(5-bromopentyl)-3-(3,4-dichlorophenyl)-, (2E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

603152-34-7

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603152-34-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 603152-34-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,3,1,5 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 603152-34:
(8*6)+(7*0)+(6*3)+(5*1)+(4*5)+(3*2)+(2*3)+(1*4)=107
107 % 10 = 7
So 603152-34-7 is a valid CAS Registry Number.

603152-34-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(5-bromopentyl)-3-(3,4-dichlorophenyl)prop-2-enamide

1.2 Other means of identification

Product number -
Other names 2-Propenamide,N-(5-bromopentyl)-3-(3,4-dichlorophenyl)-,(2E)

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:603152-34-7 SDS

603152-34-7Downstream Products

603152-34-7Relevant academic research and scientific papers

Synthesis and structure-activity relationships of 3-phenyl-2-propenamides as inhibitors of glycogen phosphorylase a

Li, Yue H.,Coppo, Frank T.,Evans, Karen A.,Graybill, Todd L.,Patel, Mehul,Gale, Jennifer,Li, Hu,Tavares, Francis,Thomson, Stephen A.

, p. 5892 - 5896 (2007/10/03)

A series of 3-phenyl-2-propenamides discovered from a high-throughput screening campaign as novel, potent, glucose-sensitive inhibitors of human liver glycogen phosphorylase a is described. A solid-phase synthesis on DMHB resin was also developed which pr

CCR2: Characterization of the antagonist binding site from a combined receptor modeling/mutagenesis approach

Berkhout, Theo A.,Blaney, Frank E.,Bridges, Angela M.,Cooper, David G.,Forbes, Ian T.,Gribble, Andrew D.,Groot, Pieter H. E.,Hardy, Adam,Ife, Robert J.,Kaur, Rejbinder,Moores, Kitty E.,Shillito, Helen,Willetts, Jennifer,Witherington, Jason

, p. 4070 - 4086 (2007/10/03)

We describe here a classical molecular modeling exercise that was carried out to provide a basis for the design of novel antagonist ligands of the CCR2 receptor. Using a theoretical model of the CCR2 receptor, docking studies were carried out to define pl

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