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2-(2',6'-dihydroxybenzoyl)-3-methylpyrrole O,O-diacetate is a complex organic compound with the molecular formula C16H15NO6. It is derived from the pyrrole class of heterocyclic compounds, characterized by a five-membered ring containing one nitrogen atom and four carbon atoms. In this specific compound, the pyrrole ring is substituted with a methyl group at the 3-position and a 2',6'-dihydroxybenzoyl group at the 2-position. The dihydroxybenzoyl moiety is further acetylated at both hydroxyl groups, resulting in the O,O-diacetate structure. 2-(2',6'-dihydroxybenzoyl)-3-methylpyrrole O,O-diacetate is known for its potential applications in various fields, including pharmaceuticals and materials science, due to its unique chemical properties and reactivity.

79205-23-5

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79205-23-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79205-23-5 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, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 79205-23:
(7*7)+(6*9)+(5*2)+(4*0)+(3*5)+(2*2)+(1*3)=135
135 % 10 = 5
So 79205-23-5 is a valid CAS Registry Number.

79205-23-5Downstream Products

79205-23-5Relevant 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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