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53241-62-6

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53241-62-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53241-62-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,2,4 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 53241-62:
(7*5)+(6*3)+(5*2)+(4*4)+(3*1)+(2*6)+(1*2)=96
96 % 10 = 6
So 53241-62-6 is a valid CAS Registry Number.

53241-62-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(dimethylamino)-2-phenylindene-1-thione

1.2 Other means of identification

Product number -
Other names 3-dimethylamino-2-phenylindene-1-thione

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:53241-62-6 SDS

53241-62-6Relevant articles and documents

Hydrothiolysis of carbofunctional α,β-unsaturated sulfides as an approach to the synthesis of 1,7-dithiocarbonyl compounds

Timokhina,Sokol'nikova,Kanitskaya,Yashchenko,Toryashinova,Voronkov

, p. 1208 - 1212 (2007/10/03)

Bis(1-N,N-dimethylimmonio-3-phenylprop-2-en-3-yl) sulfide diperchlorate and (1-N,N-dimethyl-immonio-3-phenylprop-2-en-3-yl) (5,5-dimethyl-1- morpholiniocyclohex-2-en-3-yl) sulfide diperchlorate react with hydrogen sulfide giving rise to the corresponding

α,β-UNSATURATED THIO COMPOUNDS. SYNTHESIS AND SOME CHEMICAL TRANSFORMATIONS OF THE THIO DERIVATIVES OF 2-ARYL-1-INDANONES AND 2-ARYL-1,3-INDANEDIONES

Petriashvili, K. A.,Usov, V. A.,Voronkov, M. G.

, p. 507 - 512 (2007/10/02)

In the reaction of 2-aryl-1-indanones and 2-aryl-1,3-indanediones with hydrogen sulfide in the presence of hydrogen chloride 2-aryl-3-indenethiols and 3-mercapto-2-aryl-1-indenethiones respectively are formed.The latter are readily acylated, condense with

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