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4,5-Thiazoledione, 2-(4-chlorophenyl)-, also known as 2-(4-Chlorophenyl)-4,5-thiazolidinedione, is a chemical compound with the molecular formula C8H5ClNO2S. It is a white to off-white crystalline solid and is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. 4,5-Thiazoledione, 2-(4-chlorophenyl)- is characterized by its thiazolidinedione core, which is a five-membered heterocyclic ring containing sulfur, oxygen, and nitrogen atoms, and a 4-chlorophenyl group attached to the 2-position. Due to its potential applications in the development of drugs and pesticides, it is an important compound in the field of medicinal chemistry and chemical research.

3553-58-0

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3553-58-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3553-58-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,5 and 3 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3553-58:
(6*3)+(5*5)+(4*5)+(3*3)+(2*5)+(1*8)=90
90 % 10 = 0
So 3553-58-0 is a valid CAS Registry Number.

3553-58-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-chlorophenyl)-1,3-thiazole-4,5-dione

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:3553-58-0 SDS

3553-58-0Relevant academic research and scientific papers

Facile synthesis of 2-azaazulenes from thiobenzoyl isocyanates using trimethylsilyldiazomethane

Morita, Mikio,Hari, Yoshiyuki,Iguchi, Tomoe,Aoyama, Toyohiko

, p. 1753 - 1758 (2008/09/17)

The reaction of trimethylsilyldiazomethane with thiobenzoyl isocyanates, in situ generated from thiazole-4,5-diones, yielded diazoketones, which were converted into 2-azaazulenes by the intramolecular Buchner reaction.

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