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CAS 131707-24-9

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Ethyl 6-bromo-5-hydroxy-1-methyl-2-[(phenylthio)methyl]-1H-indole-3-carboxylate

Description:
Ethyl 6-bromo-5-hydroxy-1-methyl-2-[(phenylthio)methyl]-1H-indole-3-carboxylate is a complex organic 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 bromo group at the 6-position and a hydroxy group at the 5-position contributes to its reactivity and potential biological activity. The ethyl ester functional group at the carboxylate position enhances its solubility in organic solvents, making it suitable for various applications in organic synthesis and medicinal chemistry. The phenylthio group introduces additional steric and electronic properties, which may influence the compound's interactions with biological targets. This compound may exhibit interesting pharmacological properties, although specific biological activities would require further investigation. Overall, its unique structural features suggest potential utility in research, particularly in the fields of drug discovery and development.
Formula:C19H18BrNO3S
InChI:InChI=1S/C19H18BrNO3S/c1-3-24-19(23)18-13-9-17(22)14(20)10-15(13)21(2)16(18)11-25-12-7-5-4-6-8-12/h4-10,22H,3,11H2,1-2H3
InChI key:InChIKey=DAFNNZWQTJQQAP-UHFFFAOYSA-N
SMILES:C(OCC)(=O)C=1C=2C(N(C)C1CSC3=CC=CC=C3)=CC(Br)=C(O)C2
Synonyms:
  • 1-Methyl-2-phenylthiomethyl-3-ethoxycarbonyl-5-hydroxy-6-bromoindole
  • 1H-Indole-3-carboxylic acid, 6-bromo-5-hydroxy-1-methyl-2-[(phenylthio)methyl]-, ethyl ester
  • 6-bromo-5-hydroxy-1-methyl-2-phenyl S-methyl indole-3-carboxylic acid ethyl ester
  • Ethyl 6-bromo-5-hydroxy-1-methyl-2-[(phenylthio)methyl]-1H-indole-3-carboxylate
  • Ethyl 6-bromo-5-hydroxy-1-methyl-2-phenylthiomethylindole-3-Carboxylate
  • Ethyl6-Bromo-6-Hydroxy-1-Methyl-2-((Phenylthio)Methyl)Ind.
  • SI 5 (pharmaceutical)
  • ethyl 6-bromo-5-hydroxy-1-methyl-2-[(phenylsulfanyl)methyl]-1H-indole-3-carboxylate
  • SI 5
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