CAS 132911-42-3
:1H-Pyrrole-2-carboxamide, N-methyl-
Description:
1H-Pyrrole-2-carboxamide, N-methyl- is an organic compound characterized by its pyrrole ring structure, which is a five-membered aromatic heterocycle containing one nitrogen atom. The presence of a carboxamide functional group at the 2-position of the pyrrole ring contributes to its chemical reactivity and potential biological activity. The N-methyl substitution indicates that a methyl group is attached to the nitrogen atom of the amide, which can influence the compound's solubility and interaction with biological targets. This compound may exhibit properties typical of both pyrrole derivatives and amides, such as potential antimicrobial or anti-inflammatory activities. Its molecular structure allows for various applications in medicinal chemistry and materials science. Additionally, the compound's stability, solubility in organic solvents, and reactivity with other chemical species can be influenced by the specific functional groups present. Overall, 1H-Pyrrole-2-carboxamide, N-methyl- is of interest for its potential applications in pharmaceuticals and research.
Formula:C6H8N2O
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Found 3 products.
N-Methyl-1H-pyrrole-2-carboxamide
CAS:<p>N-Methyl-1H-pyrrole-2-carboxamide</p>Purity:97%Molecular weight:124.14g/molN-Methyl-1H-pyrrole-2-carboxamide
CAS:<p>N-Methyl-1H-pyrrole-2-carboxamide is a synthetic molecule that inhibits the glycosylase activity of pbr322 DNA. This inhibition has been shown to be reversible, and can be reversed by a 1:1 mixture of N-methyl-1H-pyrrole-2-carboxamide and glycosylase. The inhibitory activity of N-methyl-1H-pyrrole-2 carboxamide is due to its ability to bind to the subunits of the enzyme, thereby preventing it from binding to the DNA substrate. It has been shown that this compound can also inhibit protein synthesis in vitro, although this effect is not seen in vivo.</p>Formula:C6H8N2OPurity:Min. 95%Molecular weight:124.14 g/mol
