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CAS 868755-69-5

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2-(3-Chlorophenyl)-4-thiazolecarbonyl chloride

Description:
2-(3-Chlorophenyl)-4-thiazolecarbonyl chloride is a chemical compound characterized by its thiazole and chlorophenyl functional groups. It features a thiazole ring, which is a five-membered heterocyclic structure containing both sulfur and nitrogen atoms, contributing to its reactivity and potential biological activity. The presence of the carbonyl chloride functional group indicates that it is an acyl chloride, making it reactive towards nucleophiles, which can be utilized in various synthetic applications. The 3-chlorophenyl substituent enhances its lipophilicity and may influence its interaction with biological targets. This compound is typically used in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, due to its ability to serve as an acylating agent. Safety precautions should be taken when handling this compound, as acyl chlorides can be corrosive and may release hydrochloric acid upon reaction with water. Overall, 2-(3-Chlorophenyl)-4-thiazolecarbonyl chloride is a versatile intermediate in chemical synthesis with potential applications in medicinal chemistry.
Formula:C10H5Cl2NOS
InChI:InChI=1S/C10H5Cl2NOS/c11-7-3-1-2-6(4-7)10-13-8(5-15-10)9(12)14/h1-5H
InChI key:InChIKey=PBAOKEBRFVHPSM-UHFFFAOYSA-N
SMILES:C(Cl)(=O)C=1N=C(SC1)C2=CC(Cl)=CC=C2
Synonyms:
  • 2-(3-Chlorophenyl)-4-thiazolecarbonyl chloride
  • 4-Thiazolecarbonyl chloride, 2-(3-chlorophenyl)-
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