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191474-79-0

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191474-79-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 191474-79-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,4,7 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 191474-79:
(8*1)+(7*9)+(6*1)+(5*4)+(4*7)+(3*4)+(2*7)+(1*9)=160
160 % 10 = 0
So 191474-79-0 is a valid CAS Registry Number.

191474-79-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,7-dimethoxybenzothiazolyl-2-carbonitrile

1.2 Other means of identification

Product number -
Other names 4,7-dimethoxybenzothiazole-2-carbonitrile

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:191474-79-0 SDS

191474-79-0Upstream product

191474-79-0Relevant articles and documents

Synthesis and in vitro antitumour evaluation of benzothiazole-2- carbonitrile derivatives

Beneteau, Valerie,Besson, Thierry,Guillard, Jerome,Leonce, Stephane,Pfeiffer, Bruno

, p. 1053 - 1060 (1999)

Novel benzothiazole derivatives have been synthesised via the corresponding imino-1,2,3-dithiazoles. The cytotoxicity of some of these polyheterocyclic compounds was studied. Our results show that 2-cyano derivatives exhibit a medium in vitro antitumour a

Eco-Friendly Microwave-Assisted Scaleable Synthesis of 2-Cyanobenzothiazoles via N-Arylimino-1,2,3-dithiazoles

Frere, Stephane,Thiery, Valerie,Besson, Thierry

, p. 3795 - 3804 (2007/10/03)

The cyclization procedure of N-aryl iminodithiazoles into 2-cyanobenzothiazoles was re-investigated with the aim to develop original and environmentally friendly procedures. In this article, the benefits associated with the microwave methodology are reported and the opportunity to use solvent-free procedures in order to scale up organic synthesis is studied. The result obtained show that the strong thermal effects due to graphite/microwaves interaction can be efficiently used for the synthesis of heterocyclic molecules for which traditional methods failed or are less attractive.

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