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CAS 175202-28-5

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3-Chloro-4-[(1-methylethyl)sulfonyl]-2-thiophenecarbonyl chloride

Description:
3-Chloro-4-[(1-methylethyl)sulfonyl]-2-thiophenecarbonyl chloride is a chemical compound characterized by its unique structure, which includes a thiophene ring, a carbonyl chloride functional group, and a sulfonyl group attached to an isopropyl moiety. This compound typically exhibits properties associated with both aromatic and heterocyclic compounds, such as stability and reactivity due to the presence of the electron-withdrawing carbonyl and sulfonyl groups. The chlorine atom contributes to its electrophilic character, making it a potential candidate for various chemical reactions, including nucleophilic substitutions. The presence of the thiophene ring may impart specific electronic properties and enhance its solubility in organic solvents. Additionally, this compound may be of interest in pharmaceutical and agrochemical applications due to its potential biological activity. As with many chlorinated compounds, it is essential to handle it with care, considering its reactivity and potential environmental impact. Proper safety measures should be observed when working with this substance in a laboratory setting.
Formula:C8H8Cl2O3S2
InChI:InChI=1S/C8H8Cl2O3S2/c1-4(2)15(12,13)5-3-14-7(6(5)9)8(10)11/h3-4H,1-2H3
InChI key:InChIKey=IECIGDCEDBXRTI-UHFFFAOYSA-N
SMILES:S(C(C)C)(=O)(=O)C=1C(Cl)=C(C(Cl)=O)SC1
Synonyms:
  • 2-Thiophenecarbonyl chloride, 3-chloro-4-[(1-methylethyl)sulfonyl]-
  • 3-Chloro-4-[(1-Methylethyl)Sulfonyl]Thiophene-2-Carbonyl Chloride
  • 3-Chloro-4-[(1-methylethyl)sulfonyl]-2-thiophenecarbonyl chloride
  • 3-Chloro-4-propan-2-ylsulfonyl-2-thiophenecarbonyl chloride
  • 3-Chloro-4-(isopropylsulfonyl)thiophene-2-carbonyl chloride
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