113602-62-3

Basic information

• Product Name: 1H-Pyrrole-2-carboxylic acid, 3-hydroxy-1-Methyl-, Methyl ester
• Synonyms: 1H-Pyrrole-2-carboxylic acid, 3-hydroxy-1-Methyl-, Methyl ester;Methyl 3-hydroxy-1-Methyl-1H-pyrrole-2-carboxylate
• CAS NO: 113602-62-3
• Molecular Formula: C7H9NO3
• Molecular Weight: 155.15126
• EINECS: -0
• Mol File: 113602-62-3.mol
• Article Data: 3

Chemical Properties

• Melting Point: 44-46 °C(Solv: pentane (109-66-0))
• Boiling Point: 61-64 °C(Press: 0.5 Torr)
• Appearance: /
• Density: 1.22±0.1 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 10.66±0.15(Predicted)
• CAS DataBase Reference: 1H-Pyrrole-2-carboxylic acid, 3-hydroxy-1-Methyl-, Methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrrole-2-carboxylic acid, 3-hydroxy-1-Methyl-, Methyl ester(113602-62-3)
• EPA Substance Registry System: 1H-Pyrrole-2-carboxylic acid, 3-hydroxy-1-Methyl-, Methyl ester(113602-62-3)

Safety Data

• Hazardous Substances Data: 113602-62-3(Hazardous Substances Data)

Usage

General Description

1H-Pyrrole-2-carboxylic acid, 3-hydroxy-1-methyl-, methyl ester is a chemical compound with the molecular formula C7H9NO3. It is a methyl ester of 3-hydroxy-1-methyl-1H-pyrrole-2-carboxylic acid, and it is commonly used in the field of organic synthesis and pharmaceuticals. 1H-Pyrrole-2-carboxylic acid, 3-hydroxy-1-methyl-, methyl ester has potential pharmacological properties and may be used in the development of new drugs. It is also used as a building block for the synthesis of various organic compounds. Additionally, it has been studied for its potential role in the treatment of certain medical conditions, making it a compound of interest in the field of medicinal chemistry.

Upstream product

• 74-89-5 methylamine 
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• 150713-74-9 methyl 5-chloro-3-oxo-2-(triphenylphosphoranylidene)pentanoate 

Downstream Products

• 113589-14-3 4,5-dibromo-3-(1-methylethoxy)-1-methyl-N-1H-tetrazol-5-yl-1 H-pyrrole-2-carboxamide 

Relevant articles and documents

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

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

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.