ethyl 2-amino-1,3-thiazole-4-carboxylate
$300.00
CAS No.: 127942-30-7
Catalog No.: 194935
Purity: 95%
MF: C6H8N2O2S
MW: 172.209
Storage: 2-8 degree Celsius
SMILES: NC=1SC=C(N1)C(=O)OCC
Catalog No.: 194935
Purity: 95%
MF: C6H8N2O2S
MW: 172.209
Storage: 2-8 degree Celsius
SMILES: NC=1SC=C(N1)C(=O)OCC
ethyl 2-amino-1,3-thiazole-4-carboxylate; CAS No.: 127942-30-7; ethyl 2-amino-1,3-thiazole-4-carboxylate. PROPERTIES: ethyl 2-amino-1,3-thiazole-4-carboxylate is a crystalline solid. Its molecular formula is C7H9N2O3S, and the molecular weight is approximately 215.23 g/mol. The compound has a melting point of approximately 100-102 C. It is moderately soluble in common organic solvents such as methanol and ethyl acetate, but is poorly soluble in water. For proper storage, it should be kept in a sealed container at room temperature, away from heat and direct sunlight. As a compound containing a thiazole ring, an amino group, and an ester group, it may exhibit certain reactivity and stability. When handling it, protective gloves and eye protection should be worn. In case of accidental contact with skin or eyes, immediate rinsing with water is necessary. APPLICATIONS: In organic synthesis, ethyl 2-amino-1,3-thiazole-4-carboxylate serves as a valuable intermediate. The amino group can undergo various reactions such as acylation, sulfonation, and diazotization. The ester group can be hydrolyzed to a carboxylic acid. In the pharmaceutical industry, derivatives of this compound can be explored as potential drug candidates. For example, in the development of certain antimicrobial agents, the structure of ethyl 2-amino-1,3-thiazole-4-carboxylate can be modified to enhance the drug's antimicrobial activity and selectivity (as reported in medicinal chemistry journals). Additionally, in the field of chemical research, it can be used as a starting material for the synthesis of novel organic compounds with potential applications in catalysis and sensing (as mentioned in organic chemistry research papers).
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