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126193-43-9

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126193-43-9 Usage

General Description

1-(5-chloro-2-phenyl-1H-indol-3-yl)thiourea is a chemical compound with the molecular formula C15H11ClN2S. It is a thiourea derivative with a substituted 1H-indole ring, containing a chlorine atom at the 5-position and a phenyl group at the 2-position. Thiourea compounds are known for their diverse biological and pharmaceutical activities, including antiviral, antitumor, and antimicrobial properties. 1-(5-chloro-2-phenyl-1H-indol-3-yl)thiourea may have potential applications in medicinal and pharmaceutical research due to its unique structure and potential biological activities. Further research is needed to fully understand its properties and potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 126193-43-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,1,9 and 3 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 126193-43:
(8*1)+(7*2)+(6*6)+(5*1)+(4*9)+(3*3)+(2*4)+(1*3)=119
119 % 10 = 9
So 126193-43-9 is a valid CAS Registry Number.

126193-43-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (5-chloro-2-phenyl-1H-indol-3-yl)thiourea

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

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More Details:126193-43-9 SDS

126193-43-9Relevant articles and documents

Synthesis of indolothiazoles and indolothiazolidinones

Hiremath, S. P.,Bajji, A. C.,Biradar, J. S.

, p. 824 - 828 (2007/10/02)

Various N-(2-phenyl-3-indolyl)thioureas (3a-d) on reaction with monochloroacetic acid and α-haloketones afford 2-phenyl-3-(4'-oxothiazolidin-2'-ylimino)indoles (4a-d) and 2-phenyl-3-(4'-substituted-2'-thiazolylamino)indoles (5a-d), respectively.The amides

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