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CAS 91348-45-7

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3-bromoindole-2-carboxylic acid ethyl eater

Description:
3-Bromoindole-2-carboxylic acid ethyl ester is a chemical compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. The presence of a bromine atom at the 3-position of the indole ring introduces a halogen substituent, which can influence the compound's reactivity and biological activity. The carboxylic acid functional group at the 2-position, along with the ethyl ester moiety, suggests that this compound can participate in various chemical reactions, including esterification and hydrolysis. This compound is likely to exhibit moderate solubility in organic solvents due to its hydrophobic indole core, while the carboxylic acid group may impart some polar characteristics. Additionally, compounds of this type are often studied for their potential pharmacological properties, including antimicrobial and anticancer activities, due to the biological significance of indole derivatives. Safety and handling precautions should be observed, as with many brominated compounds, due to potential toxicity and environmental concerns.
Formula:C11H10BrNO2
InChI:InChI=1/C11H10BrNO2/c1-2-15-11(14)10-9(12)7-5-3-4-6-8(7)13-10/h3-6,13H,2H2,1H3
SMILES:CCOC(=O)c1c(c2ccccc2[nH]1)Br
Synonyms:
  • 1H-Indole-2-carboxylic acid, 3-bromo-, ethyl ester
  • Ethyl 3-bromo-1H-indole-2-carboxylate
  • 3-Bromoindole-2-carboxylic acid ethyl ester
  • 3-Bromo-1H-Indole-2-Carboxylic Acid Ethyl Ester
  • Ethyl 3-Bromoindole-2-Carboxylate
  • 3-Bromo-2-IndolecarboxylicAcidEthylEster
  • 3-Br-ICA-OEt
  • ETHYL 3-BROMOINDOL-2-CARBOXYLATE
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