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CAS 64837-49-6

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Ethyl 5-chloro-1,3,4-thiadiazole-2-carboxylate

Description:
Ethyl 5-chloro-1,3,4-thiadiazole-2-carboxylate is a heterocyclic compound characterized by the presence of a thiadiazole ring, which incorporates sulfur and nitrogen atoms. This compound features a carboxylate functional group, contributing to its reactivity and potential applications in organic synthesis. The chlorine atom at the 5-position of the thiadiazole ring enhances its electrophilic properties, making it useful in various chemical reactions, including nucleophilic substitutions. Ethyl 5-chloro-1,3,4-thiadiazole-2-carboxylate is often utilized in the development of agrochemicals, pharmaceuticals, and as an intermediate in the synthesis of other complex organic molecules. Its solubility in organic solvents and moderate stability under standard conditions make it a versatile building block in synthetic chemistry. Additionally, the presence of the ethyl ester group can influence its biological activity and solubility profile, making it a subject of interest in medicinal chemistry and drug development. Overall, this compound exemplifies the diverse applications of thiadiazole derivatives in various fields of chemistry.
Formula:C5H5ClN2O2S
InChI:InChI=1/C5H5ClN2O2S/c1-2-10-4(9)3-7-8-5(6)11-3/h2H2,1H3
SMILES:CCOC(=O)c1nnc(Cl)s1
Synonyms:
  • 1,3,4-Thiadiazole-2-Carboxylic Acid, 5-Chloro-, Ethyl Ester
  • Ethyl 5-chloro-1,3,4-thiadiazole-2-carboxylate
  • 5-Chloro-1,3,4-thiadiazole-2-carboxylate ethyl ester
  • 5-Chloro-[1,3,4]Thiadiazole-2-Carboxylicacid Ethyl Ester
  • 1,3,4-Thiadiazole-2-carboxylicacid, 5-chloro-, ethyl ester
  • Ethyl 2-Chloro-1,3,4-Thiadiazole-5-Carboxylate
  • 114187
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