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CAS 40731-16-6

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5-chloro-3-methyl-1H-indole-2-carbaldehyde

Description:
5-Chloro-3-methyl-1H-indole-2-carbaldehyde is an 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 chloro group at the 5-position and a methyl group at the 3-position contributes to its unique reactivity and properties. The aldehyde functional group at the 2-position makes it a versatile intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its reactivity is influenced by the electron-withdrawing nature of the chloro group and the electron-donating properties of the methyl group, which can affect its behavior in various chemical reactions, such as nucleophilic additions or condensation reactions. Safety data should be consulted for handling, as with many organic compounds, it may pose health risks if not managed properly.
Formula:C10H8ClNO
InChI:InChI=1/C10H8ClNO/c1-6-8-4-7(11)2-3-9(8)12-10(6)5-13/h2-5,12H,1H3
SMILES:Cc1c2cc(ccc2[nH]c1C=O)Cl
Synonyms:
  • 1H-indole-2-carboxaldehyde, 5-chloro-3-methyl-
  • 5-CHLORO-3-METHYL-1H-INDOLE-2-CARBALDEHYDE
  • 5-chloro-3-methyl-1H-indole-2-carbaldehyde(SALTDATA: 0.1H2O)
  • 5-chloro-3-methyl-1H-indole-2-carboxaldehyde
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