Methyl 4,6-dimethoxy-2-indolecarboxylate is an organic compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This particular compound features two methoxy groups (-OCH3) at the 4 and 6 positions of the indole ring, contributing to its unique chemical properties and reactivity. The presence of the carboxylate group (-COOCH3) at the 2 position enhances its potential for various chemical reactions, including esterification and nucleophilic substitutions. Methyl 4,6-dimethoxy-2-indolecarboxylate is often utilized in organic synthesis and medicinal chemistry due to its ability to serve as a building block for more complex molecules. Its solubility in organic solvents and moderate stability under standard laboratory conditions make it a valuable compound in research settings. Additionally, the methoxy groups can influence the compound's electronic properties, potentially affecting its biological activity and interactions with other molecules. Overall, this compound exemplifies the diverse chemistry associated with indole derivatives.

methyl 4,6-dimethoxy-2-indolecarboxylate

105776-13-4: Methyl 4,6-dimethoxy-2-indolecarboxylate is an organic compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This particular compound features two methoxy groups (-OCH3) at the 4 and 6 positions of the indole ring, contributing to its unique chemical properties and reactivity. The presence of the carboxylate group (-COOCH3) at the 2 position enhances its potential for various chemical reactions, including esterification and nucleophilic substitutions. Methyl 4,6-dimethoxy-2-indolecarboxylate is often utilized in organic synthesis and medicinal chemistry due to its ability to serve as a building block for more complex molecules. Its solubility in organic solvents and moderate stability under standard laboratory conditions make it a valuable compound in research settings. Additionally, the methoxy groups can influence the compound's electronic properties, potentially affecting its biological activity and interactions with other molecules. Overall, this compound exemplifies the diverse chemistry associated with indole derivatives.

CAS 105776-13-4

methyl 4,6-dimethoxy-2-indolecarboxylate

Methyl 4,6-dimethoxy-1H-indole-2-carboxylate

Ref: IN-DA008540

Methyl 4,6-dimethoxy-2-indolecarboxylate

Ref: 7W-GK4202

METHYL 4,6-DIMETHOXY-1H-INDOLE-2-CARBOXYLATE

Ref: 10-F531530

Methyl 4,6-dimethoxy-1H-indole-2-carboxylate

Ref: 3D-FEA77613