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1H-Pyrrole-3-carboxylic acid, 2-(2-mercaptophenyl)-1-phenyl-, also known as 2-(2-mercaptophenyl)-1-phenyl-1H-pyrrole-3-carboxylic acid, is a complex organic compound with the molecular formula C16H13NOS2. 1H-Pyrrole-3-carboxylic acid, 2-(2-mercaptophenyl)-1-phenyl- features a pyrrole ring, which is a five-membered aromatic ring containing one nitrogen atom, and a carboxylic acid group attached to the third position of the pyrrole. Additionally, it has a phenyl group (a benzene ring) and a 2-mercaptophenyl group (a benzene ring with a thiol group at the second position) attached to the second position of the pyrrole ring. This chemical structure endows the compound with unique properties and potential applications in various fields, such as pharmaceuticals, materials science, and chemical research.

88264-04-4

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88264-04-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88264-04-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,2,6 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 88264-04:
(7*8)+(6*8)+(5*2)+(4*6)+(3*4)+(2*0)+(1*4)=154
154 % 10 = 4
So 88264-04-4 is a valid CAS Registry Number.

88264-04-4SDS

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 1-phenyl-2-(2-sulfanylphenyl)pyrrole-3-carboxylic acid

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

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More Details:88264-04-4 SDS

88264-04-4Downstream Products

88264-04-4Relevant academic research and scientific papers

Cyclisation of α-(2-mercaptobenzoyl)- and α-(2-aminobenzoyl)lactames; Synthesis of benzothiopyranopyrrolinones and pyrrolinoquinolinones

Eiden,Baumann

, p. 897 - 907 (2007/10/02)

Compounds 8a, 8b, 8d, 8e and 8f are obtained by heating the mercaptobenzoyl- or methylaminobenzoyl-lactames 6a, 6b, 6d, 6e and 6f. With pyridine HCl removal of the pyrroline N-methyl group takes place under formation of 8c and 8g. Cyclisation of the acyll

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