Ethyl 2-methyl-1H-indole-3-carboxylate, with the CAS number 53855-47-3, is an organic compound that belongs to the class of indole derivatives. It features a carboxylate functional group and an ethyl ester, contributing to its chemical reactivity and potential applications in organic synthesis. The indole structure is characterized by a fused bicyclic system containing a benzene ring and a pyrrole ring, which imparts unique electronic properties and biological activity. This compound is typically a colorless to pale yellow liquid or solid, depending on its purity and form. It is soluble in organic solvents, such as ethanol and dichloromethane, but has limited solubility in water. Ethyl 2-methyl-1H-indole-3-carboxylate may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry. Its synthesis often involves multi-step reactions, including the formation of the indole core and subsequent esterification. As with many organic compounds, proper handling and safety precautions are essential due to potential toxicity and reactivity.

ethyl 2-methyl-1H-indole-3-carboxylate

53855-47-3: 1H-indole-3-carboxylic acid, 2-methyl-, ethyl ester,  Ethyl 2-methyl-1H-indole-3-carboxylate

ETHYL 2-METHYL-2,3-DIHYDRO-INDOLE-3-CARBOXYLATE

Ethyl 2-methylindole-3-carboxylate is a multisubstituted indole that is produced by the catalyzed reaction of ethyl acetoacetate and potassium carbonate. This compound contains two methyl groups, one carboxyl group, and one carboxylic acid group. Ethyl 2-methylindole-3-carboxylate is obtained by heating the corresponding ketone in a sealed tube with potassium carbonate, producing the desired product as a white solid. The yield of this reaction is about 82%.

CAS 53855-47-3: ethyl 2-methyl-1H-indole-3-carboxylate

ETHYL 2-METHYL-2,3-DIHYDRO-INDOLE-3-CARBOXYLATE

Ref: IN-DA00DBNC

Ethyl 2-methylindole-3-carboxylate

Ref: 3D-FE170483

Ethyl 2-methyl-1H-indole-3-carboxylate

Ref: 10-F364000

Ethyl 2-methyl-1H-indole-3-carboxylate

Ref: 54-OR74876