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CAS 860624-88-0

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1H-Indole-7-carboxylic acid, 5-bromo-2,3-dihydro-, methyl ester

Description:
1H-Indole-7-carboxylic acid, 5-bromo-2,3-dihydro-, methyl ester, identified by CAS number 860624-88-0, is a chemical compound that features an indole ring structure, which is a bicyclic compound consisting of a benzene fused to a pyrrole. This compound is characterized by the presence of a carboxylic acid functional group and a methyl ester, indicating it can undergo hydrolysis to yield the corresponding acid. The bromine substitution at the 5-position of the indole ring introduces unique electronic and steric properties, potentially influencing its reactivity and biological activity. The dihydro form suggests that the compound may exhibit reduced aromaticity compared to fully aromatic indoles, which can affect its stability and interactions. This compound may be of interest in medicinal chemistry and research due to its potential biological activities, including antimicrobial or anticancer properties, stemming from the indole scaffold's known pharmacological significance. As with many organic compounds, proper handling and safety measures should be observed due to potential toxicity or reactivity.
Formula:C10H10BrNO2
InChI:InChI=1S/C10H10BrNO2/c1-14-10(13)8-5-7(11)4-6-2-3-12-9(6)8/h4-5,12H,2-3H2,1H3
InChI key:InChIKey=AXFDCMFCJPYARR-UHFFFAOYSA-N
SMILES:C(OC)(=O)C1=C2C(=CC(Br)=C1)CCN2
Synonyms:
  • Methyl 5-bromoindoline-7-carboxylate
  • 1H-Indole-7-carboxylic acid, 5-bromo-2,3-dihydro-, methyl ester
  • Methyl 5-bromo-2,3-dihydro-1H-indole-7-carboxylate
  • 5-BROMO-INDOLINE-7-CARBOXYLIC ACID METHYL ESTER
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