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CAS 153501-30-5

:

ethyl 5-bromo-3-hydroxy-1H-indole-2-carboxylate

Description:
Ethyl 5-bromo-3-hydroxy-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 a bromine atom at the 5-position and a hydroxyl group at the 3-position of the indole ring, contributing to its reactivity and potential biological activity. The presence of the ethyl ester group at the 2-carboxylate position enhances its solubility in organic solvents and may influence its pharmacokinetic properties. The compound is of interest in medicinal chemistry due to its potential applications in drug development, particularly in the context of indole derivatives, which are known for various biological activities, including anti-inflammatory and anticancer properties. Its molecular structure allows for various synthetic modifications, making it a versatile intermediate in organic synthesis. As with many brominated compounds, it may exhibit unique reactivity patterns, particularly in electrophilic substitution reactions. Safety and handling precautions should be observed due to the presence of bromine and the potential for biological activity.
Formula:C11H10BrNO3
InChI:InChI=1/C11H10BrNO3/c1-2-16-11(15)9-10(14)7-5-6(12)3-4-8(7)13-9/h3-5,13-14H,2H2,1H3
SMILES:CCOC(=O)c1c(c2cc(ccc2[nH]1)Br)O
Synonyms:
  • 1H-Indole-2-carboxylic acid, 5-bromo-3-hydroxy-, ethyl ester
  • Ethyl 5-bromo-3-hydroxy-1H-indole-2-carboxylate
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