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CAS 78468-68-5

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ethyl (2-amino-4-methyl-1,3-thiazol-5-yl)acetate

Description:
Ethyl (2-amino-4-methyl-1,3-thiazol-5-yl)acetate is an organic compound characterized by its thiazole ring, which contributes to its biological activity and potential applications in pharmaceuticals. The thiazole moiety contains both sulfur and nitrogen, providing unique reactivity and properties. This compound features an ethyl acetate functional group, which enhances its solubility in organic solvents and may influence its interaction with biological systems. The presence of the amino group suggests potential for hydrogen bonding, which can affect its pharmacokinetics and binding affinity to biological targets. Ethyl (2-amino-4-methyl-1,3-thiazol-5-yl)acetate may exhibit various biological activities, making it of interest in medicinal chemistry. Its molecular structure allows for potential modifications that could enhance its efficacy or reduce toxicity. As with many thiazole derivatives, it may be investigated for applications in areas such as antimicrobial or anticancer research. Safety and handling precautions should be observed, as with any chemical substance, due to potential hazards associated with its use.
Formula:C8H12N2O2S
InChI:InChI=1/C8H12N2O2S/c1-3-12-7(11)4-6-5(2)10-8(9)13-6/h3-4H2,1-2H3,(H2,9,10)
SMILES:CCOC(=O)Cc1c(C)[nH]c(=N)s1
Synonyms:
  • 5-Thiazoleacetic Acid, 2-Amino-4-Methyl-, Ethyl Ester
  • Ethyl 2-(2-amino-4-methylthiazol-5-yl)acetate
  • Ethyl 2-(2-amino-4-methyl-1,3-thiazol-5-yl)acetate
  • ethyl (2-amino-4-methyl-1,3-thiazol-5-yl)acetate
  • (2-amino-4-methylthiazol-5-yl)acetic acid ethyl ester
  • ethyl (2-amino-4-methyl-1,3-thiazol-5-yl)acetate(SALTDATA: FREE)
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