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CAS 19749-93-0

:

ethyl 2-(2-chloroacetamido)-4-thiazole-acetate

Description:
Ethyl 2-(2-chloroacetamido)-4-thiazole-acetate is a chemical compound characterized by its thiazole ring, which contributes to its biological activity. The presence of the chloroacetamido group indicates potential reactivity and interaction with biological targets, making it of interest in medicinal chemistry. This compound typically exhibits moderate solubility in organic solvents and may have limited solubility in water due to its hydrophobic thiazole structure. Its molecular structure suggests potential applications in pharmaceuticals, particularly in the development of antimicrobial or anti-inflammatory agents. The acetate group may enhance its lipophilicity, facilitating membrane permeability. Additionally, the compound's stability and reactivity can be influenced by environmental factors such as pH and temperature. Overall, ethyl 2-(2-chloroacetamido)-4-thiazole-acetate is a compound of interest for further research, particularly in the context of drug development and synthesis.
Formula:C9H11ClN2O3S
InChI:InChI=1/C9H11ClN2O3S/c1-2-15-8(14)3-6-5-16-9(11-6)12-7(13)4-10/h5H,2-4H2,1H3,(H,11,12,13)
SMILES:CCOC(=O)Cc1csc(n1)N=C(CCl)O
Synonyms:
  • Ethyl 2-(2-chloroacetamido)-4-thiazoleacetate
  • Ethyl {2-[(Chloroacetyl)Amino]-1,3-Thiazol-4-Yl}Acetate
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