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2-(2',6'-dimethoxybenzoyl)-4-methylpyrrole is a complex organic compound with the molecular formula C15H15NO4. It is characterized by a pyrrole ring, which is a five-membered aromatic ring containing one nitrogen atom, and a 4-methyl substituent, indicating a methyl group attached to the pyrrole ring at the 4-position. The compound also features a 2',6'-dimethoxybenzoyl group, which is a benzoyl group (a benzene ring with a carbonyl group) that has two methoxy groups (-OCH3) attached at the 2' and 6' positions. This structure is significant in the field of organic chemistry and may have potential applications in the synthesis of pharmaceuticals or other chemical products due to its unique electronic and steric properties.

79205-15-5

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79205-15-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79205-15-5 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, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 79205-15:
(7*7)+(6*9)+(5*2)+(4*0)+(3*5)+(2*1)+(1*5)=135
135 % 10 = 5
So 79205-15-5 is a valid CAS Registry Number.

79205-15-5Downstream Products

79205-15-5Relevant 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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