CAS 935-72-8
:1H-Pyrrole-3,4-dicarboxylic acid
Description:
1H-Pyrrole-3,4-dicarboxylic acid, with the CAS number 935-72-8, is an organic compound characterized by its pyrrole ring structure, which is a five-membered aromatic heterocycle containing nitrogen. This compound features two carboxylic acid functional groups (-COOH) located at the 3 and 4 positions of the pyrrole ring, contributing to its acidic properties. It is typically a white to off-white solid that is soluble in water and polar organic solvents, owing to the presence of the carboxylic acid groups. The compound is of interest in various fields, including organic synthesis and materials science, due to its potential applications in the development of pharmaceuticals, agrochemicals, and as a building block for more complex molecules. Its reactivity is influenced by the electron-rich nature of the pyrrole ring, making it a suitable candidate for electrophilic substitution reactions. Additionally, the presence of multiple functional groups allows for further derivatization, enhancing its utility in chemical synthesis.
Formula:C6H5NO4
Synonyms:- 1H-pyrrole-3,4-dicarboxylic acid
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 4 products.
1H-pyrrole-3,4-dicarboxylic acid
CAS:Controlled ProductFormula:C6H5NO4Color and Shape:NeatMolecular weight:155.11H-Pyrrole-3,4-dicarboxylic acid
CAS:<p>1H-Pyrrole-3,4-dicarboxylic acid is a benzyl substituted derivative of pyrrole that exhibits photophysical properties in the visible region of the spectrum. The crystal structure is composed of a hexagonal unit cell with a lattice parameter of 2.914 Å, containing one molecule in the asymmetric unit. It has been shown to undergo cycloaddition reactions with azomethine ylides to form 1,3-dipolar adducts. Substituent effects on the reactivity and photophysical properties have been evaluated by comparing 1H-pyrrole-3,4-dicarboxylic acid with its diethyl ester and sterically hindered carboxy analogues.</p>Formula:C6H5NO4Purity:Min. 95%Molecular weight:155.11 g/mol
