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650606-13-6

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650606-13-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 650606-13-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,0,6,0 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 650606-13:
(8*6)+(7*5)+(6*0)+(5*6)+(4*0)+(3*6)+(2*1)+(1*3)=136
136 % 10 = 6
So 650606-13-6 is a valid CAS Registry Number.

650606-13-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(ethoxymethyl)-3-(4-hexoxyphenyl)prop-2-enenitrile

1.2 Other means of identification

Product number -
Other names 2-Propenenitrile,2-(ethoxymethyl)-3-[4-(hexyloxy)phenyl]-,(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:650606-13-6 SDS

650606-13-6Relevant articles and documents

2,4-Diaminopyrimidines as inhibitors of leishmanial and trypanosomal dihydrofolate reductase

Pez, Didier,Leal, Isabel,Zuccotto, Fabio,Boussard, Cyrille,Brun, Reto,Croft, Simon L.,Yardley, Vanessa,Ruiz Perez, Luis M.,Gonzalez Pacanowska, Dolores,Gilbert, Ian H.

, p. 4693 - 4711 (2007/10/03)

This paper describes the synthesis of 4′-substituted and 3′,4′-disubstituted 5-benzyl-2,4-diaminopyrimidines as selective inhibitors of leishmanial and trypanosomal dihydrofolate reductase. Compounds were then assayed against the recombinant parasite and human enzymes. Some of the compounds showed good activity. They were also tested against the intact parasites using in vitro assays. Good activity was found against Trypanosoma cruzi, moderate activity against Trypanosoma brucei and Leishmania donovani. Molecular modeling was undertaken to explain the results. The leishmanial enzyme was found to have a more extensive lipophilic binding region in the active site than the human enzyme. Compounds which bound within the pocket showed the highest selectivity.

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