Methyl 4-formyl-2,5-dimethyl-1H-pyrrole-3-carboxylate is an organic compound characterized by its pyrrole ring structure, which is a five-membered aromatic heterocycle containing nitrogen. This compound features a formyl group (-CHO) and a carboxylate ester group (-COOCH3) attached to the pyrrole ring, contributing to its reactivity and potential applications in organic synthesis. The presence of two methyl groups at the 2 and 5 positions of the pyrrole enhances its hydrophobicity and may influence its electronic properties. This compound is typically a solid or liquid at room temperature, depending on its purity and specific conditions. It may exhibit moderate solubility in organic solvents such as ethanol and dichloromethane, while being less soluble in water due to its non-polar characteristics. Methyl 4-formyl-2,5-dimethyl-1H-pyrrole-3-carboxylate can be utilized in various chemical reactions, including condensation and substitution reactions, making it valuable in the synthesis of more complex organic molecules, particularly in the fields of pharmaceuticals and agrochemicals.

methyl 4-formyl-2,5-dimethyl-1H-pyrrole-3-carboxylate

175205-91-1: Methyl 4-formyl-2,5-dimethyl-1H-pyrrole-3-carboxylate is an organic compound characterized by its pyrrole ring structure, which is a five-membered aromatic heterocycle containing nitrogen. This compound features a formyl group (-CHO) and a carboxylate ester group (-COOCH3) attached to the pyrrole ring, contributing to its reactivity and potential applications in organic synthesis. The presence of two methyl groups at the 2 and 5 positions of the pyrrole enhances its hydrophobicity and may influence its electronic properties. This compound is typically a solid or liquid at room temperature, depending on its purity and specific conditions. It may exhibit moderate solubility in organic solvents such as ethanol and dichloromethane, while being less soluble in water due to its non-polar characteristics. Methyl 4-formyl-2,5-dimethyl-1H-pyrrole-3-carboxylate can be utilized in various chemical reactions, including condensation and substitution reactions, making it valuable in the synthesis of more complex organic molecules, particularly in the fields of pharmaceuticals and agrochemicals.

CAS 175205-91-1

methyl 4-formyl-2,5-dimethyl-1H-pyrrole-3-carboxylate

1H-Pyrrole-3-carboxylic acid, 4-formyl-2,5-dimethyl-, methyl ester

Ref: IN-DA0020PC

Methyl 2,5-dimethyl-4-formyl-1H-pyrrole-3-carboxylate

Ref: 54-OR29452

Methyl 4-formyl-2,5-dimethyl-1H-pyrrole-3-carboxylate

Ref: 10-F635802