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CAS 16382-18-6

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Ethyl 5,6-dimethoxy-1H-indole-2-carboxylate

Description:
Ethyl 5,6-dimethoxy-1H-indole-2-carboxylate is a chemical compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This specific compound features two methoxy groups (-OCH3) attached to the 5 and 6 positions of the indole ring, contributing to its unique reactivity and solubility properties. The ethyl ester functional group at the 2-position enhances its potential for various chemical reactions, including esterification and hydrolysis. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents such as ethanol and dichloromethane. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to the biological activity often associated with indole derivatives. Additionally, the presence of methoxy groups can influence the compound's electronic properties, potentially affecting its interaction with biological targets. As with many organic compounds, safety precautions should be observed when handling this substance, including the use of appropriate personal protective equipment.
Formula:C13H15NO4
InChI:InChI=1S/C13H15NO4/c1-4-18-13(15)10-5-8-6-11(16-2)12(17-3)7-9(8)14-10/h5-7,14H,4H2,1-3H3
InChI key:InChIKey=RBUSDPZPBBBAKR-UHFFFAOYSA-N
SMILES:C(OCC)(=O)C1=CC=2C(N1)=CC(OC)=C(OC)C2
Synonyms:
  • 1H-Indole-2-carboxylic acid, 5,6-dimethoxy-, ethyl ester
  • 5,6-Dimethoxy-1H-indole-2-carboxylic acid ethyl ester
  • Ethyl 5,6-dimethoxy-2-indolecarboxylate
  • Ethyl 5,6-dimethoxyindole-2-carboxylate
  • Indole-2-carboxylic acid, 5,6-dimethoxy-, ethyl ester
  • ethyl 5,6-dimethoxy-1H-indole-2-carboxylate
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