Ethyl 4-phenyl-1,2,3-thiadiazole-5-carboxylate is a chemical compound characterized by its unique structure, which includes a thiadiazole ring fused with a phenyl group and an ethyl ester functional group. This compound typically exhibits properties associated with heterocyclic compounds, such as moderate solubility in organic solvents and potential reactivity due to the presence of the thiadiazole moiety. The thiadiazole ring contributes to its potential biological activity, making it of interest in medicinal chemistry and drug development. Ethyl 4-phenyl-1,2,3-thiadiazole-5-carboxylate may also display interesting optical properties, which can be exploited in various applications, including materials science and organic electronics. Its synthesis often involves multi-step reactions, and it can be characterized using techniques such as NMR spectroscopy, mass spectrometry, and infrared spectroscopy to confirm its structure and purity. Overall, this compound represents a versatile building block in organic synthesis and has potential applications in pharmaceuticals and agrochemicals.

ethyl 4-phenyl-1,2,3-thiadiazole-5-carboxylate

58756-26-6: Ethyl 4-phenyl-1,2,3-thiadiazole-5-carboxylate is a chemical compound characterized by its unique structure, which includes a thiadiazole ring fused with a phenyl group and an ethyl ester functional group. This compound typically exhibits properties associated with heterocyclic compounds, such as moderate solubility in organic solvents and potential reactivity due to the presence of the thiadiazole moiety. The thiadiazole ring contributes to its potential biological activity, making it of interest in medicinal chemistry and drug development. Ethyl 4-phenyl-1,2,3-thiadiazole-5-carboxylate may also display interesting optical properties, which can be exploited in various applications, including materials science and organic electronics. Its synthesis often involves multi-step reactions, and it can be characterized using techniques such as NMR spectroscopy, mass spectrometry, and infrared spectroscopy to confirm its structure and purity. Overall, this compound represents a versatile building block in organic synthesis and has potential applications in pharmaceuticals and agrochemicals.

CAS 58756-26-6

ethyl 4-phenyl-1,2,3-thiadiazole-5-carboxylate

ethyl 4-phenyl-1,2,3-thiadiazole-5-carboxylate

Ref: 54-OR23653

4-Phenyl-[1,2,3]thiadiazole-5-carboxylic acid ethyl ester

Ref: 10-F316911