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CAS 34859-65-9

:

ethyl 5-amino-3-methylisothiazole-4-carboxylate

Description:
Ethyl 5-amino-3-methylisothiazole-4-carboxylate is a chemical compound characterized by its isothiazole ring structure, which contributes to its unique reactivity and properties. This compound features an amino group, a carboxylate functional group, and an ethyl ester, making it a versatile intermediate in organic synthesis. It is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the presence of the carboxylate group. The isothiazole moiety is known for its biological activity, often serving as a scaffold in the development of pharmaceuticals and agrochemicals. The compound may also display properties such as antimicrobial or antifungal activity, which are common in derivatives of isothiazole. Safety data should be consulted for handling, as with any chemical, to ensure proper precautions are taken. Overall, ethyl 5-amino-3-methylisothiazole-4-carboxylate is a significant compound in medicinal chemistry and synthetic applications.
Formula:C7H10N2O2S
InChI:InChI=1/C7H10N2O2S/c1-3-11-7(10)5-4(2)9-12-6(5)8/h3,8H2,1-2H3
SMILES:CCOC(=O)c1c(C)nsc1N
Synonyms:
  • 4-Isothiazolecarboxylic Acid, 5-Amino-3-Methyl-, Ethyl Ester
  • Ethyl 5-amino-3-methyl-1,2-thiazole-4-carboxylate
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