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Acetamide, N-(3-chlorophenyl)-2-[[[1-[(4-cyanophenyl)methyl]-1H-imidazol-5-yl]meth yl](2-hydroxyethyl)amino]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

253862-99-6

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253862-99-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 253862-99-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,3,8,6 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 253862-99:
(8*2)+(7*5)+(6*3)+(5*8)+(4*6)+(3*2)+(2*9)+(1*9)=166
166 % 10 = 6
So 253862-99-6 is a valid CAS Registry Number.

253862-99-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(3-Chlorophenyl)-N2-{[1-(4-cyanobenzyl)-1H-imidazol-5-yl]methyl}-N2-(2-hydroxyethyl)glycinamide

1.2 Other means of identification

Product number -
Other names -

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:253862-99-6 SDS

253862-99-6Relevant articles and documents

Preparation of a clinically investigated ras farnesyl transferase inhibitor

Maligres, Peter E.,Waters, Marjorie S.,Weissman, Steven A.,McWilliams, J. Christopher,Lewis, Stephanie,Cowen, Jennifer,Reamer, Robert A.,Volante,Reider, Paul J.,Askin, David

, p. 229 - 241 (2007/10/03)

The synthesis of ras farnesyl-protein transferase inhibitor 1 is described on a multi-kilogram scale. Retrosynthetic analysis reveals chloromethylimidazole 2 and a piperazinone 3 as viable precursors. The 1,5-disubstituted imidazole system was regioselectively assembled via an improved Marckwald imidazole synthesis. A new imidazole dethionation procedure has been developed to convert the Marckwald mercaptoimidazole product to the desired imidazole. This methodology was found to be tolerant of a variety of functional groups providing good to excellent yields of 1,5-disubstituted imidazoles. A new Mitsunobu cyclization strategy was developed to prepare the arylpiperazinone fragment 3.

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