5-Phenyl-1,2,3-thiadiazole is a heterocyclic organic compound characterized by a five-membered ring containing two nitrogen atoms and one sulfur atom, along with a phenyl group attached to the carbon backbone. This compound typically exhibits a pale yellow to light brown appearance and is known for its aromatic properties due to the presence of the phenyl group. It is soluble in organic solvents, which makes it useful in various chemical applications. The thiadiazole ring contributes to its potential biological activity, making it of interest in medicinal chemistry and material science. Additionally, 5-phenyl-1,2,3-thiadiazole can participate in various chemical reactions, including nucleophilic substitutions and cycloadditions, due to the reactivity of the nitrogen and sulfur atoms. Its derivatives may exhibit diverse pharmacological properties, including antimicrobial and anti-inflammatory activities. Overall, this compound serves as a valuable building block in the synthesis of more complex organic molecules and has potential applications in pharmaceuticals and agrochemicals.

5-phenyl-1,2,3-thiadiazole

18212-29-8: 5-Phenyl-1,2,3-thiadiazole is a heterocyclic organic compound characterized by a five-membered ring containing two nitrogen atoms and one sulfur atom, along with a phenyl group attached to the carbon backbone. This compound typically exhibits a pale yellow to light brown appearance and is known for its aromatic properties due to the presence of the phenyl group. It is soluble in organic solvents, which makes it useful in various chemical applications. The thiadiazole ring contributes to its potential biological activity, making it of interest in medicinal chemistry and material science. Additionally, 5-phenyl-1,2,3-thiadiazole can participate in various chemical reactions, including nucleophilic substitutions and cycloadditions, due to the reactivity of the nitrogen and sulfur atoms. Its derivatives may exhibit diverse pharmacological properties, including antimicrobial and anti-inflammatory activities. Overall, this compound serves as a valuable building block in the synthesis of more complex organic molecules and has potential applications in pharmaceuticals and agrochemicals.

CAS 18212-29-8

5-phenyl-1,2,3-thiadiazole

1,2,3-Thiadiazole, 5-phenyl-

Ref: IN-DA0023EQ

5-Phenyl-[1,2,3]thiadiazole

Ref: 54-OR346390

5-Phenyl-1,2,3-thiadiazole

Ref: 10-F018971