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2-(2',6'-dimethoxybenzoyl)-3-phenylpyrrole is a complex organic compound characterized by a pyrrole ring, which is a five-membered aromatic ring containing four carbon atoms and 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 the benzoyl group itself has two methoxy substituents (-OCH3) at the 2' and 6' positions. Additionally, a phenyl group (a benzene ring) is attached to the pyrrole at the 3-position. This molecule is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds due to its unique structure and reactivity.

79205-20-2

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79205-20-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79205-20-2 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 0 respectively.
Calculate Digit Verification of CAS Registry Number 79205-20:
(7*7)+(6*9)+(5*2)+(4*0)+(3*5)+(2*2)+(1*0)=132
132 % 10 = 2
So 79205-20-2 is a valid CAS Registry Number.

79205-20-2Relevant 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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