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1H-Pyrrole-2-carboxylic acid, 3-acetyl-4,5-dimethyl-, ethyl ester is a complex organic compound with the chemical formula C12H15NO3. It is a derivative of pyrrole, a heterocyclic aromatic organic compound consisting of a five-membered ring with four carbon atoms and one nitrogen atom. In this specific compound, the pyrrole ring is substituted with a carboxylic acid group at the 2-position, an acetyl group at the 3-position, and two methyl groups at the 4 and 5 positions. The ethyl ester group is attached to the carboxylic acid, making it a derivative of the parent acid. 1H-Pyrrole-2-carboxylic acid, 3-acetyl-4,5-dimethyl-, ethyl ester is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its role as an intermediate in organic chemistry. Its unique structure and functional groups make it an interesting target for researchers in the field of organic synthesis and drug development.

2386-32-5

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2386-32-5 Usage

Structure

Ethyl ester derivative of 1H-pyrrole-2-carboxylic acid with acetyl and dimethyl substituents

Usage

Building block in organic synthesis and in the production of various drugs and pharmaceutical intermediates

Applications

Potential use in medicinal chemistry and drug discovery

Versatility

Diverse potential uses in organic synthesis and pharmaceutical research.

Check Digit Verification of cas no

The CAS Registry Mumber 2386-32-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,8 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2386-32:
(6*2)+(5*3)+(4*8)+(3*6)+(2*3)+(1*2)=85
85 % 10 = 5
So 2386-32-5 is a valid CAS Registry Number.

2386-32-5Relevant academic research and scientific papers

PREPARATION OF 4,5-DIALKYL-3-ACYL-PYRROLE-2-CARBOXYLIC ACID DERIVATIVES BY FISCHER-FINK TYPE SYNTHESIS AND SUBSEQUENT ACYLATION

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Page/Page column 21-24, (2008/06/13)

The present invention relates to an improved synthesis of pyrrole capping group precursors of formula I-a: comprising: combining an aqueous solution of the compound of formula IV-a: wherein R3 is C1-12 aliphatic, C3-12 alkyl-cycloaliphatic, C3-12 alkyl-aryl, C3-12 alkyl-heteroaryl, or C3-12 alkyl-cycloaliphatic; with a compound of formula V-a, wherein R1 and R2 are each independently C1-6 aliphatic; in the presence of zinc, water, and optionally an additional suitable solvent to form a compound of formula VI.

A NEW METHOD FOR THE PRODUCTION OF PYRROLYLACETYLENES

Kozhich, D. T.,Vasilevskii, V. I.,Mironov, A. F.,Evstigneeva, R. P.

, p. 745 - 750 (2007/10/02)

A new method was developed for the production of a previously difficulty obtainable class of pyrroles, i.e., pyrrolylacetylenes.The method is based on the discovered reaction between alkyl pyrrolyl ketones and phosphorus oxychloride in dimethylformamide, as a result of which α-chloroalkenylpyrroles are formed.The latter are converted by the action of alkali into pyrrolylacetylenes with high yields.When twice the amount of phosphorus oxychloride is used α-chloro-β-formylvinylpyrroles are formed.The stereochemistry of these compounds was studied.

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