CAS 111698-89-6: ETHYL 3-ALLYL-4-AMINO-2-THIOXO-2,3-DIHYDRO-1,3-THIAZOLE-5-CARBOXYLATE

Description: Ethyl 3-allyl-4-amino-2-thioxo-2,3-dihydro-1,3-thiazole-5-carboxylate, with the CAS number 111698-89-6, is a chemical compound characterized by its thiazole ring structure, which incorporates both sulfur and nitrogen atoms. This compound features an ethyl ester functional group, contributing to its solubility properties. The presence of an allyl group indicates potential reactivity, particularly in addition reactions or polymerization processes. The thioxo group (C=S) enhances its reactivity and may influence its biological activity, making it of interest in medicinal chemistry. The amino group (-NH2) can participate in hydrogen bonding and may enhance the compound's interaction with biological targets. Overall, this compound's unique structural features suggest potential applications in pharmaceuticals, agrochemicals, or as a building block in organic synthesis. However, specific properties such as melting point, boiling point, and solubility would require empirical data for precise characterization.

Formula: C₉H₁₂N₂O₂S₂

5-Thiazolecarboxylicacid, 4-amino-2,3-dihydro-3-(2-propen-1-yl)-2-thioxo-, ethyl ester

CAS: 111698-89-6

• Formula: C₉H₁₂N₂O₂S₂
• Molecular weight: 244.3338

Ethyl 4-amino-3-(prop-2-en-1-yl)-2-sulfanylidene-2,3-dihydro-1,3-thiazole-5-carboxylate

CAS: 111698-89-6

• Purity: 97%
• Molecular weight: 244.3300018310547

Ethyl 3-allyl-4-amino-2-thioxo-2,3-dihydro-1,3-thiazole-5-carboxylate

CAS: 111698-89-6

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• Formula: C₉H₁₂N₂O₂S₂
• Purity: Min. 95%
• Molecular weight: 244.34 g/mol