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CAS 69812-29-9

:

2-Acetamido-4-methyl-5-thiazolesulfonyl chloride

Description:
2-Acetamido-4-methyl-5-thiazolesulfonyl chloride, with the CAS number 69812-29-9, is a chemical compound characterized by its thiazole ring structure, which incorporates both an acetamido group and a sulfonyl chloride functional group. This compound typically appears as a solid or crystalline substance and is known for its reactivity due to the presence of the sulfonyl chloride moiety, which can participate in nucleophilic substitution reactions. It is often utilized in organic synthesis, particularly in the preparation of various thiazole derivatives and other bioactive compounds. The thiazole ring contributes to its potential biological activity, making it of interest in medicinal chemistry. Additionally, the compound's solubility and stability can vary depending on the solvent and environmental conditions. Safety precautions should be observed when handling this substance, as sulfonyl chlorides can be corrosive and may release toxic gases upon reaction with water or amines. Overall, 2-Acetamido-4-methyl-5-thiazolesulfonyl chloride is a valuable intermediate in chemical synthesis with specific applications in research and development.
Formula:C6H7ClN2O3S2
InChI:InChI=1S/C6H7ClN2O3S2/c1-3-5(14(7,11)12)13-6(8-3)9-4(2)10/h1-2H3,(H,8,9,10)
InChI key:InChIKey=NXGKPRKPUCSEIL-UHFFFAOYSA-N
SMILES:S(Cl)(=O)(=O)C=1SC(NC(C)=O)=NC1C
Synonyms:
  • 2-(Acetylamino)-4-Methyl-1,3-Thiazole-5-Sulfonyl Chloride
  • 2-(Acetylamino)-4-methyl-5-thiazolesulfonyl chloride
  • 2-Acetamido-4-Methylthiazole-5-Sulfonyl Chloride
  • 2-Acetamido-4-methyl-1,3-thiazole-5-sulfonyl chloride
  • 2-Acetamido-4-methyl-5-thiazolesulfonyl chloride
  • 2-Acetylamino-4-Methyl-Thiazole-5-Sulfonyl Chloride
  • 5-Thiazolesulfonyl chloride, 2-(acetylamino)-4-methyl-
  • 5-Thiazolesulfonyl chloride, 2-acetamido-4-methyl-
  • NSC 95414
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