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CAS 22980-10-5

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1H-Indole-3-acetyl chloride, 2-methyl-a-oxo-

Description:
1H-Indole-3-acetyl chloride, 2-methyl-a-oxo- is a chemical compound characterized by its indole structure, which is a bicyclic compound consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. The presence of an acetyl chloride functional group indicates that it is a derivative of acetic acid, where the hydroxyl group is replaced by a chlorine atom, making it a reactive acyl chloride. This compound is typically used in organic synthesis, particularly in the preparation of various indole derivatives and other complex organic molecules. Its reactivity is attributed to the electrophilic nature of the carbonyl carbon in the acetyl chloride group, which can participate in nucleophilic acyl substitution reactions. Additionally, the methyl group at the 2-position of the indole ring can influence the compound's reactivity and stability. As with many acyl chlorides, it is important to handle this compound with care due to its potential to release hydrochloric acid upon reaction and its sensitivity to moisture.
Formula:C11H8ClNO2
InChI:InChI=1S/C11H8ClNO2/c1-6-9(10(14)11(12)15)7-4-2-3-5-8(7)13-6/h2-5,13H,1H3
InChI key:InChIKey=MBAONGDWDAMRIY-UHFFFAOYSA-N
SMILES:C(C(Cl)=O)(=O)C=1C=2C(NC1C)=CC=CC2
Synonyms:
  • 2-Methyl-α-oxo-1H-indole-3-acetyl chloride
  • Indole-3-glyoxyloyl chloride, 2-methyl-
  • 1H-Indole-3-acetyl chloride, 2-methyl-α-oxo-
  • 2-(2-Methyl-1H-indol-3-yl)-2-oxoacetyl chloride
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