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CAS 13632-07-0

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5-acetamido-2-methylbenzenesulphonyl chloride

Description:
5-Acetamido-2-methylbenzenesulphonyl chloride, with the CAS number 13632-07-0, is an organic compound characterized by the presence of both an acetamido group and a sulphonyl chloride functional group. This compound typically appears as a solid or crystalline substance and is known for its reactivity due to the sulphonyl chloride moiety, which can participate in nucleophilic substitution reactions. The acetamido group contributes to its solubility in polar solvents and can influence its biological activity. It is often utilized in organic synthesis, particularly in the preparation of sulfonamides and other derivatives. The compound's structure includes a methyl group, which can affect its steric properties and reactivity. Safety precautions are necessary when handling this substance, as sulphonyl chlorides can be corrosive and may release toxic gases upon reaction with water or alcohols. Overall, 5-acetamido-2-methylbenzenesulphonyl chloride is a valuable intermediate in chemical synthesis and pharmaceutical applications.
Formula:C9H10ClNO3S
InChI:InChI=1/C9H10ClNO3S/c1-6-3-4-8(11-7(2)12)5-9(6)15(10,13)14/h3-5H,1-2H3,(H,11,12)
InChI key:InChIKey=BCGUUSFEJVCVLK-UHFFFAOYSA-N
SMILES:S(Cl)(=O)(=O)C1=CC(NC(C)=O)=CC=C1C
Synonyms:
  • 3′-(Chlorosulfonyl)aceto-p-toluidide
  • 5-(Acetylamino)-2-Methylbenzenesulfonyl Chloride
  • Benzenesulfonyl chloride, 5-(acetylamino)-2-methyl-
  • o-Toluenesulfonyl chloride, 5-acetamido-
  • 5-Acetamido-2-methylbenzenesulphonyl chloride
  • 5-AcetaMido-2-Methylbenzene-1-sulfonyl chloride
  • Einecs 237-118-9
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