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1H-Pyrrole-1-carboxylic acid, 2,5-dihydro-2-(2-oxopropyl)-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

380367-23-7

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380367-23-7 Usage

Molecular structure

1H-Pyrrole-1-carboxylic acid, 2,5-dihydro-2-(2-oxopropyl)-, methyl ester consists of a pyrrole ring with a carboxylic acid group at one position and a methyl ester at another position, along with a 2,5-dihydro-2-(2-oxopropyl) moiety.

Functional groups

The compound contains a pyrrole ring, carboxylic acid group, methyl ester group, and a 2-oxopropyl group.

Potential applications

This chemical compound has potential applications in the fields of organic synthesis, pharmaceuticals, and materials science.

Versatile building block

Due to its unique structure and functional groups, it serves as a versatile building block for the synthesis of various organic compounds.

Biological activities

The compound may possess potential biological activities, but further research and testing are required to confirm and understand its properties and uses.

Check Digit Verification of cas no

The CAS Registry Mumber 380367-23-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,0,3,6 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 380367-23:
(8*3)+(7*8)+(6*0)+(5*3)+(4*6)+(3*7)+(2*2)+(1*3)=147
147 % 10 = 7
So 380367-23-7 is a valid CAS Registry Number.

380367-23-7Downstream Products

380367-23-7Relevant academic research and scientific papers

Synthesis of 2,3-disubstituted pyrrolidines and piperidines via one-pot oxidative decarboxylation-β-iodination of amino acids

Boto,Hernandez,De Leon,Suarez

, p. 7796 - 7803 (2001)

A new synthesis of 2,3-disubstituted pyrrolidines and piperidines is described. This mild procedure is based on the one-pot oxidative decarboxylation-β -iodination of α-amino acid carbamates or amides. The iodine is introduced at the previously unfunction

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