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51361-17-2

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51361-17-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51361-17-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,3,6 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 51361-17:
(7*5)+(6*1)+(5*3)+(4*6)+(3*1)+(2*1)+(1*7)=92
92 % 10 = 2
So 51361-17-2 is a valid CAS Registry Number.

51361-17-2SDS

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 2-methyl-N-(2,2,2-trichloro-1-hydroxyethyl)benzamide

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:51361-17-2 SDS

51361-17-2Upstream product

51361-17-2Relevant articles and documents

Potassium channel openers

-

, (2008/06/13)

Compounds of formula I: are useful in treating diseases prevented by or ameliorated with potassium channel openers. Also disclosed are potassium channel opening compositions and a method of opening potassium channels in a mammal.

New Derivatives of Asymmetic Chloral Aminals.

Barczynski,Eckstein

, p. 176 - 177 (2007/10/09)

This paper is concerned by newly developed fungicides. In the reported research program, first there were prepared parent carboxylic acids of benodanil, mebenil, furcarbanil, pyracarbolid, carboxin and G-696. Then they were transformed into respective amides. From the latter, by action of chloral, its semiaminals were obtained. Under analogous conditions, for the purpose of comparison in future tests on biological activity, chloral semiaminals were prepared from amides of the following acids: phenylthio - and phenylsulfoacetic, 3-(2 prime -chlorophenyl) - and 3-(2 prime ,6 prime -dichlorophenyl) - 5 -methylisoxazolcarboxylic-4. By action of phenyl isocyanate, 4-chlorophenyl and 3,4-dichlorophenyl on all chloral semiaminals synthesized respective asymmetric aminals of this aldehyde were obtained. The above reactions run with carbon dioxide elimination and give high yields of products.

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