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CAS 323580-68-3

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tert-butyl 6-chloroindole-1-carboxylate

Description:
Tert-butyl 6-chloroindole-1-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. The presence of a tert-butyl group enhances its lipophilicity, making it more soluble in organic solvents. The chloro substituent at the 6-position of the indole ring introduces a halogen, which can influence the compound's reactivity and biological activity. The carboxylate functional group, derived from the carboxylic acid, is typically involved in esterification reactions and can participate in various chemical transformations. This compound may be of interest in medicinal chemistry and drug development due to its potential biological activities, including antimicrobial or anticancer properties. Its specific characteristics, such as melting point, boiling point, and spectral data, would be determined through experimental methods and can vary based on purity and environmental conditions. Overall, tert-butyl 6-chloroindole-1-carboxylate represents a versatile scaffold for further chemical modifications and applications in research.
Formula:C13H14ClNO2
InChI:InChI=1/C13H14ClNO2/c1-13(2,3)17-12(16)15-7-6-9-4-5-10(14)8-11(9)15/h4-8H,1-3H3
SMILES:CC(C)(C)OC(=O)n1ccc2ccc(cc12)Cl
Synonyms:
  • tert-Butyl 6-chloro-1H-indole-1-carboxylate
  • 6-Chloroindole, N-BOC protected 98%
  • 6-Chloroindole, N-BOC protected
  • 1-BOC-6-CHLOROINDOLE
  • 6-chloro-1-indolecarboxylic acid tert-butyl ester
  • 6-Chloroindole-1-carboxylic acid tert-butyl ester
  • tert-butyl 6-chloro-1H-indole-3-carboxylate
  • 1-Boc-6-chloro-1H-indole
  • 6-Chloroindole,N-BOCprotected98%
  • 1H-Indole-1-carboxylic acid, 6-chloro-, 1,1-dimethylethyl ester
  • BOC-6-CHLOROINDOLE
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