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2-(2',6'-dihydroxybenzoyl)-3-phenylpyrrole O,O-diacetate is a complex organic compound with the molecular formula C20H15NO6. It is characterized by a pyrrole ring, which is a five-membered aromatic ring containing one nitrogen atom, and a phenyl group attached to the pyrrole. The compound also features a 2',6'-dihydroxybenzoyl group, which is a derivative of benzoic acid with two hydroxyl groups at the 2' and 6' positions. The O,O-diacetate part of the name indicates that two acetate groups are attached to the molecule, typically to the hydroxyl groups, forming ester linkages. 2-(2',6'-dihydroxybenzoyl)-3-phenylpyrrole O,O-diacetate is known for its potential applications in various fields, including pharmaceuticals and materials science, due to its unique structure and properties.

79205-24-6

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79205-24-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79205-24-6 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 79205-24:
(7*7)+(6*9)+(5*2)+(4*0)+(3*5)+(2*2)+(1*4)=136
136 % 10 = 6
So 79205-24-6 is a valid CAS Registry Number.

79205-24-6Relevant 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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