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104692-80-0

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104692-80-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104692-80-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,6,9 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 104692-80:
(8*1)+(7*0)+(6*4)+(5*6)+(4*9)+(3*2)+(2*8)+(1*0)=120
120 % 10 = 0
So 104692-80-0 is a valid CAS Registry Number.

104692-80-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl N'-cyano-N-(phenylsulfonyl)carbamimidothioate

1.2 Other means of identification

Product number -
Other names methyl N'-cyano-N-(phenylsulfonyl)imidothiocarbamate

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:104692-80-0 SDS

104692-80-0Relevant articles and documents

A novel and efficient regiospecific preparation of arenesulfonamide derivatives of 3,5-diamino-1,2,4-triazole

Chibale, Kelly,Dauvergne, Jér?me,Wyatt, Paul G.

, p. 185 - 190 (2007/10/03)

A new simple and efficient procedure was designed for the regiospecific preparation of arenesulfonamide derivatives of 3,5-diamino-1,2,4-triazole 1 which are precursors of N-([1,2,4] triazolo [1,5-a]pyrimidin-2-yl)arenesulfonamides 2, an important family of herbicidal and antibacterial agents. The key feature of this procedure is the preparation of a wide range of compounds 1 on a large scale, in pure form and high yield without the need for any workup or the use of the highly hazardous hydrazine. This was made possible by a novel tandem reaction promoted by sulfuryl chloride to effect the formation of the triazole ring.

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