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CAS 1379610-44-2

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Methyl 2-amino-5-ethyl-4-thiazoleacetate

Description:
Methyl 2-amino-5-ethyl-4-thiazoleacetate is a chemical compound characterized by its thiazole ring, which contributes to its biological activity and potential applications in pharmaceuticals. The presence of an amino group and an ethyl substituent on the thiazole ring enhances its reactivity and solubility in organic solvents. This compound typically exhibits moderate polarity due to the ester functional group, which can influence its interaction with biological systems. Methyl 2-amino-5-ethyl-4-thiazoleacetate may participate in various chemical reactions, including nucleophilic substitutions and condensation reactions, making it a versatile intermediate in organic synthesis. Additionally, compounds with thiazole structures are often investigated for their antimicrobial, antifungal, and anticancer properties, suggesting potential therapeutic applications. Safety and handling precautions should be observed, as with any chemical substance, to mitigate risks associated with exposure. Overall, the unique structural features of this compound position it as a subject of interest in both synthetic chemistry and medicinal research.
Formula:C8H12N2O2S
InChI:InChI=1S/C8H12N2O2S/c1-3-6-5(4-7(11)12-2)10-8(9)13-6/h3-4H2,1-2H3,(H2,9,10)
InChI key:InChIKey=HGZPDSOTTSAERI-UHFFFAOYSA-N
SMILES:C(C(OC)=O)C1=C(CC)SC(N)=N1
Synonyms:
  • 4-Thiazoleacetic acid, 2-amino-5-ethyl-, methyl ester
  • Methyl 2-amino-5-ethyl-4-thiazoleacetate
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