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CAS 30216-57-0

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1,3-Thiazole-2-carbonyl chloride

Description:
1,3-Thiazole-2-carbonyl chloride is a heterocyclic organic compound characterized by the presence of a thiazole ring, which is a five-membered ring containing both sulfur and nitrogen atoms. This compound features a carbonyl chloride functional group, making it a reactive acyl chloride. It typically appears as a colorless to pale yellow liquid or solid, depending on its physical state at room temperature. The presence of the carbonyl chloride group indicates that it can undergo nucleophilic acyl substitution reactions, making it useful in organic synthesis, particularly for the preparation of amides and esters. The thiazole moiety contributes to its potential biological activity, as thiazole derivatives are often found in pharmaceuticals and agrochemicals. Additionally, 1,3-thiazole-2-carbonyl chloride is sensitive to moisture and should be handled with care, as it can hydrolyze to form the corresponding carboxylic acid. Its reactivity and structural features make it a valuable intermediate in the synthesis of various chemical compounds.
Formula:C4H2ClNOS
InChI:InChI=1/C4H2ClNOS/c5-3(7)4-6-1-2-8-4/h1-2H
SMILES:c1csc(C(=O)Cl)n1
Synonyms:
  • 2-Thiazolecarbonyl Chloride
  • 1,3-Thiazole-2-carbonyl chloride
  • 1,3-Thiazole-2-carbonyl chloride 97%
  • 2-Thiazolecarbonyl chloride (8CI,9CI)
  • 2-Thiazolecarbonyl chloride (8CI, 9CI, ACI)
  • 1,3-Thiazole-2-carbonylchloride97%
  • thiazole-2-carbonyl chloride
  • 2-(Chlorocarbonyl)-1,3-thiazole, 2-(Chloroformyl)-1,3-thiazole
  • 1,3-Thiazole-2-carbonyl chloride ,95%
  • 2-(Chlorocarbonyl)-1,3-thiazole
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