4-Acetyl-3,5-dimethyl-1H-pyrrole-2-carboxylate, with the CAS number 2386-28-9, is a pyrrole derivative characterized by its unique structural features. This compound contains a pyrrole ring, which is a five-membered aromatic heterocycle containing nitrogen. The presence of acetyl and carboxylate functional groups contributes to its reactivity and potential applications in organic synthesis. Typically, compounds like this exhibit moderate solubility in organic solvents, and their reactivity can be influenced by the electron-donating and electron-withdrawing effects of the substituents on the pyrrole ring. The methyl groups at positions 3 and 5 enhance the stability of the molecule while also affecting its electronic properties. This compound may be of interest in various fields, including medicinal chemistry and materials science, due to its potential biological activity and utility in synthesizing more complex organic molecules. As with many pyrrole derivatives, it may also exhibit interesting optical and electronic properties, making it a candidate for further research and development.

4-acetyl-3,5-dimethyl-1H-pyrrole-2-carboxylate

2386-28-9: 4-Acetyl-3,5-dimethyl-1H-pyrrole-2-carboxylate, with the CAS number 2386-28-9, is a pyrrole derivative characterized by its unique structural features. This compound contains a pyrrole ring, which is a five-membered aromatic heterocycle containing nitrogen. The presence of acetyl and carboxylate functional groups contributes to its reactivity and potential applications in organic synthesis. Typically, compounds like this exhibit moderate solubility in organic solvents, and their reactivity can be influenced by the electron-donating and electron-withdrawing effects of the substituents on the pyrrole ring. The methyl groups at positions 3 and 5 enhance the stability of the molecule while also affecting its electronic properties. This compound may be of interest in various fields, including medicinal chemistry and materials science, due to its potential biological activity and utility in synthesizing more complex organic molecules. As with many pyrrole derivatives, it may also exhibit interesting optical and electronic properties, making it a candidate for further research and development.

CAS 2386-28-9

4-acetyl-3,5-dimethyl-1H-pyrrole-2-carboxylate

1H-Pyrrole-2-carboxylic acid, 4-acetyl-3,5-dimethyl-

Ref: IN-DA00I4M3

4-Acetyl-3,5-dimethyl-1H-pyrrole-2-carboxylic acid

Ref: 54-OR1005137

4-acetyl-3,5-dimethyl-1H-pyrrole-2-carboxylic acid

Ref: 10-F372259