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2-(2',6'-dihydroxybenzoyl)-3-phenylpyrrole is a complex organic compound characterized by a pyrrole ring, which is a five-membered aromatic ring containing one nitrogen atom. This particular compound features a benzoyl group (a benzene ring with a carbonyl group) attached to the pyrrole at the 2-position, and a phenyl group (a benzene ring) at the 3-position. The benzoyl group is further distinguished by two hydroxyl groups (-OH) at the 2' and 6' positions, which are para to each other on the benzene ring. This structure is significant in the field of organic chemistry and may have potential applications in various chemical and pharmaceutical industries due to its unique arrangement of functional groups.

79205-22-4

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79205-22-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79205-22-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,2,0 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 79205-22:
(7*7)+(6*9)+(5*2)+(4*0)+(3*5)+(2*2)+(1*2)=134
134 % 10 = 4
So 79205-22-4 is a valid CAS Registry Number.

79205-22-4Downstream Products

79205-22-4Relevant academic research and scientific papers

Pyoluteorin Derivatives. II. Synthetic Approaches to Pyrrole Ring Substituted Pyoluteorins (1)

Cue, Berkeley W.,Chamberlain, Nancy

, p. 667 - 670 (2007/10/02)

A method for the regiospecific synthesis of 3-substituted 2-aroylpyrroles is described.These pyrroles, which are structurally related to the naturally occuring antibiotic pyoluteorin, are prepared by a Friedel-Crafts aroylation of 4-substituted pyrrole-3-carboxylic acid esters with 2,6-dimethoxybenzoyl chloride.The carboalkoxy group is then removed by hydrolysis and decarboxylation to produce isomerically pure 3-substituted-2-(2',6'-dimethoxybenzoyl)pyrroles (5 and 13).Conversion of these pyrroles into pyoluteorin-like coumpounds led to some unexpected products which arise from facile cleavage of the dihydroxybenzoyl portion of the molecules during chlorination.

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