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CAS 35450-53-4

:

4-[2-(Acetylamino)ethyl]benzenesulfonyl chloride

Description:
4-[2-(Acetylamino)ethyl]benzenesulfonyl chloride, with the CAS number 35450-53-4, 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 a benzene ring substituted with a sulfonyl chloride group and an acetylaminoethyl side chain, contributing to its potential applications in organic synthesis and medicinal chemistry. It is typically a solid at room temperature and may exhibit a white to off-white appearance. The presence of the sulfonyl chloride group makes it a useful intermediate in the synthesis of various pharmaceuticals and agrochemicals, as it can react with amines and alcohols to form sulfonamides and other derivatives. Additionally, due to the acetylamino group, it may also exhibit biological activity, making it of interest in drug development. Proper handling and storage are essential, as sulfonyl chlorides can be reactive and may release hydrochloric acid upon hydrolysis.
Formula:C10H12ClNO3S
InChI:InChI=1/C10H12ClNO3S/c1-8(13)12-7-6-9-2-4-10(5-3-9)16(11,14)15/h2-5H,6-7H2,1H3,(H,12,13)
InChI key:InChIKey=VSHNWNOZERVVNK-UHFFFAOYSA-N
SMILES:S(Cl)(=O)(=O)C1=CC=C(CCNC(C)=O)C=C1
Synonyms:
  • 4-(2-Acetamidoethyl)benzene-1-sulfonyl chloride
  • 4-(2-Acetamidoethyl)benzenesulfonyl chloride
  • 4-(β-Acetamidoethyl)benzenesulfonyl chloride
  • 4-[2-(Acetylamino)Ethyl]Benzenesulfonyl Chloride
  • 4-[2-(N-Acetylamino)ethyl]benzenesulfonyl chloride
  • Benzenesulfonyl chloride, 4-[2-(acetylamino)ethyl]-
  • p-(2-Acetamidoethyl)benzenesulfonyl chloride
  • p-(2-acetamidoethyl)benzenesulphonyl chloride
  • 4-[2-(acetylamino)ethyl]benzenesulfonyl chloride(SALTDATA: FREE)
  • 4-(2-ACETAMIDOETHYL)BENZENE-1-SULFONYL CHLORIDE(WXG01427)
  • 4-[2-(Acetylamino)ethyl]benzenesulfonic acid chloride
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