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CAS 1452182-35-2

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4-(Aminocarbonyl)-2-thiophenesulfonyl chloride

Description:
4-(Aminocarbonyl)-2-thiophenesulfonyl 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 a thiophene ring, a five-membered aromatic heterocycle containing sulfur, which contributes to its unique electronic properties and potential applications in organic synthesis. The presence of the aminocarbonyl group indicates that it can participate in various chemical reactions, such as nucleophilic substitutions and coupling reactions, making it valuable in the synthesis of pharmaceuticals and agrochemicals. Additionally, the sulfonyl chloride moiety is often used as a versatile building block in the preparation of sulfonamides and other derivatives. The compound is typically handled with care due to its reactive nature, particularly in the presence of moisture, which can lead to hydrolysis. Overall, 4-(Aminocarbonyl)-2-thiophenesulfonyl chloride is an important intermediate in organic chemistry with potential applications in drug development and materials science.
Formula:C5H4ClNO3S2
InChI:InChI=1S/C5H4ClNO3S2/c6-12(9,10)4-1-3(2-11-4)5(7)8/h1-2H,(H2,7,8)
InChI key:InChIKey=IJFSHNBARRGHPZ-UHFFFAOYSA-N
SMILES:S(Cl)(=O)(=O)C1=CC(C(N)=O)=CS1
Synonyms:
  • 4-(Aminocarbonyl)-2-thiophenesulfonyl chloride
  • 2-Thiophenesulfonyl chloride, 4-(aminocarbonyl)-
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