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1H-Pyrrole-2-carboxylic acid, 3-hydroxy-1-methyl-, methyl ester is a chemical compound characterized by the molecular formula C7H9NO3. It is a methyl ester derivative of 3-hydroxy-1-methyl-1H-pyrrole-2-carboxylic acid, known for its potential applications in organic synthesis, pharmaceuticals, and medicinal chemistry. 1H-Pyrrole-2-carboxylic acid, 3-hydroxy-1-methyl-, methyl ester exhibits pharmacological properties, making it a promising candidate for the development of new drugs and a versatile building block for the synthesis of various organic compounds.

113602-62-3

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113602-62-3 Usage

Uses

Used in Organic Synthesis:
1H-Pyrrole-2-carboxylic acid, 3-hydroxy-1-methyl-, methyl ester is used as a building block in the synthesis of various organic compounds. Its unique structure and functional groups make it a valuable component in the creation of complex organic molecules.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 1H-Pyrrole-2-carboxylic acid, 3-hydroxy-1-methyl-, methyl ester is utilized as a key intermediate in the development of new drugs. Its pharmacological properties and potential therapeutic effects contribute to the discovery and design of innovative pharmaceutical agents.
Used in Medicinal Chemistry Research:
1H-Pyrrole-2-carboxylic acid, 3-hydroxy-1-methyl-, methyl ester is employed as a compound of interest in medicinal chemistry research. Its potential role in the treatment of certain medical conditions makes it a valuable subject for investigation and exploration in the field of drug discovery and development.
Used in Drug Synthesis for Medical Conditions:
1H-Pyrrole-2-carboxylic acid, 3-hydroxy-1-methyl-, methyl ester is used as a starting material or intermediate in the synthesis of drugs targeting specific medical conditions. Its potential therapeutic effects and pharmacological properties make it a promising candidate for the development of novel treatments and therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 113602-62-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,6,0 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 113602-62:
(8*1)+(7*1)+(6*3)+(5*6)+(4*0)+(3*2)+(2*6)+(1*2)=83
83 % 10 = 3
So 113602-62-3 is a valid CAS Registry Number.

113602-62-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-hydroxy-1-methylpyrrole-2-carboxylate

1.2 Other means of identification

Product number -
Other names 1H-Pyrrole-2-carboxylic acid,3-hydroxy-1-methyl-,methyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
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More Details:113602-62-3 SDS

113602-62-3Relevant academic research and scientific papers

Singlet oxygen in synthesis. Formation of d,l- and meso- isochrysohermidin from a 3,3'-bipyrrole precursor

Wasserman, Harry H.,Rotello, Vincent M.,Frechette, Roger,DeSimone, Robert W.,Yoo, Ji Uk,Baldino, Carmen M.

, p. 8731 - 8738 (2007/10/03)

A synthesis of the d,l and meso forms of isochrysohermidin 3 is outlined which employs the singlet oxygen oxidation of pyrroles as the key step. The bipyrrole precursor 8 was synthesized from a 3-hydroxy monopyrrole which, in turn, was prepared by additio

N-1H-tetrazol-5-yl-2-thiophene carboxamides, N-1H-tetrazol-5-yl-2-pyrrole carboxamides, N-1H-tetrazol-5-yl-2-furan carboxamides, and anti-allergic and anti-inflammatory use thereof

-

, (2008/06/13)

The present invention is for compounds having the formula of N-1H-tetrazol-5-yl-2-thiophenecarboxamides, N-1H-tetrazol-5-yl-2-pyrrolecarboxamides, N-1H-tetrazol-5-yl-2-furancarboxamides or analogs of each of the carboxamides. The compounds are useful for the treatment of allergic or inflammatory conditions or diseases. Thus, pharmaceutical compositions and methods of use are also the invention. Processes of preparation for the compounds are also the invention.

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