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CAS 52206-05-0

:

1-acetyl-2,3-dihydro-1H-indole-5-sulfonyl chloride

Description:
1-Acetyl-2,3-dihydro-1H-indole-5-sulfonyl chloride is a chemical compound characterized by its sulfonyl chloride functional group, which is known for its reactivity and ability to form sulfonamides. This compound features an indole structure, a bicyclic compound that is significant in various biological activities and synthetic applications. The presence of the acetyl group contributes to its reactivity, allowing it to participate in acylation reactions. As a sulfonyl chloride, it is typically used as a reagent in organic synthesis, particularly for the introduction of sulfonyl groups into other molecules. The compound is likely to be a solid at room temperature and may exhibit moderate to high solubility in organic solvents. It is important to handle this substance with care due to its potential reactivity and the release of hydrochloric acid upon hydrolysis. Safety precautions should be taken to avoid exposure, as sulfonyl chlorides can be irritants and may pose health risks.
Formula:C10H10ClNO3S
InChI:InChI=1/C10H10ClNO3S/c1-7(13)12-5-4-8-6-9(16(11,14)15)2-3-10(8)12/h2-3,6H,4-5H2,1H3
SMILES:CC(=O)N1CCc2cc(ccc12)S(=O)(=O)Cl
Synonyms:
  • 1-Acetylindoline-5-sulfonyl chloride
  • 1H-Indole-5-sulfonyl chloride, 1-acetyl-2,3-dihydro-
  • 1-Acetylindoline-5-sulfonylchloride,97%
  • N-ACETYLINDOLINE-5-SULPHONYL CHLORIDE
  • 1-ACETYL-5-INDOLINESULFONYL CHLORIDE
  • 1-ACETYL-2,3-DIHYDRO-1H-INDOLE-5-SULFONYL CHLORIDE
  • 1-ACETYL-5-INDOLINESULFONOYL CHLORIDE
  • N-Acetylindoline-5-sulfonyl chloride
  • 1-Acetylindoline-5-sulphonyl chloride 97%
  • 1-Acetylindoline-5-sulphonylchloride97%
  • See more synonyms
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