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CAS 175202-76-3

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5-[2-(Methylthio)-4-pyrimidinyl]-2-thiophenesulfonyl chloride

Description:
5-[2-(Methylthio)-4-pyrimidinyl]-2-thiophenesulfonyl chloride, with the CAS number 175202-76-3, is a chemical compound characterized by its unique structure that includes a pyrimidine ring and a thiophene moiety, both of which contribute to its reactivity and potential applications in medicinal chemistry. This compound features a sulfonyl chloride functional group, which is known for its high reactivity, particularly in nucleophilic substitution reactions. The presence of the methylthio group enhances its lipophilicity and may influence its biological activity. Typically, compounds of this nature are utilized in the synthesis of pharmaceuticals, agrochemicals, or as intermediates in organic synthesis due to their ability to form covalent bonds with various nucleophiles. The compound is likely to be a solid at room temperature and may require careful handling due to the reactivity of the sulfonyl chloride group, which can release hydrochloric acid upon reaction. Safety precautions should be observed when working with this substance, including the use of appropriate personal protective equipment.
Formula:C9H7ClN2O2S3
InChI:InChI=1S/C9H7ClN2O2S3/c1-15-9-11-5-4-6(12-9)7-2-3-8(16-7)17(10,13)14/h2-5H,1H3
InChI key:InChIKey=NHYJWHQTVHUETC-UHFFFAOYSA-N
SMILES:S(Cl)(=O)(=O)C=1SC(=CC1)C2=NC(SC)=NC=C2
Synonyms:
  • 2-Thiophenesulfonyl chloride, 5-[2-(methylthio)-4-pyrimidinyl]-
  • 5-(2-Methylsulfanylpyrimidin-4-yl)thiophene-2-sulfonyl chloride
  • 5-[2-(Methylsulfanyl)Pyrimidin-4-Yl]Thiophene-2-Sulfonyl Chloride
  • 5-[2-(Methylthio)-4-pyrimidinyl]-2-thiophenesulfonyl chloride
  • 5-[2-(Methylthio)pyrimidin-4-yl]thiophene-2-sulfonyl chloride
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