4-Phenyl-1,2,3-thiadiazol-5-amine is an organic compound characterized by its thiadiazole ring, which contains both nitrogen and sulfur atoms. This compound features a phenyl group attached to the thiadiazole, contributing to its aromatic properties. The presence of an amine functional group enhances its reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and coupling reactions. The thiadiazole moiety is known for its biological activity, and compounds containing this structure may exhibit antimicrobial, antifungal, or anticancer properties. Additionally, the compound's solubility and stability can vary depending on the solvent and environmental conditions. Its applications may extend to pharmaceuticals, agrochemicals, and materials science, where it could serve as a building block for more complex molecules. Safety data should be consulted to understand its handling and toxicity, as with any chemical substance. Overall, 4-phenyl-1,2,3-thiadiazol-5-amine represents a versatile structure in organic chemistry with potential applications in various fields.

4-phenyl-1,2,3-thiadiazol-5-amine

78301-72-1: 4-Phenyl-1,2,3-thiadiazol-5-amine is an organic compound characterized by its thiadiazole ring, which contains both nitrogen and sulfur atoms. This compound features a phenyl group attached to the thiadiazole, contributing to its aromatic properties. The presence of an amine functional group enhances its reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and coupling reactions. The thiadiazole moiety is known for its biological activity, and compounds containing this structure may exhibit antimicrobial, antifungal, or anticancer properties. Additionally, the compound's solubility and stability can vary depending on the solvent and environmental conditions. Its applications may extend to pharmaceuticals, agrochemicals, and materials science, where it could serve as a building block for more complex molecules. Safety data should be consulted to understand its handling and toxicity, as with any chemical substance. Overall, 4-phenyl-1,2,3-thiadiazol-5-amine represents a versatile structure in organic chemistry with potential applications in various fields.

CAS 78301-72-1

4-phenyl-1,2,3-thiadiazol-5-amine

4-Phenyl-1,2,3-thiadiazol-5-amine

Ref: IN-DA005NE4

5-Amino-4-phenyl-1,2,3-thiadiazole

Ref: 54-OR11285

4-Phenyl-1,2,3-thiadiazol-5-amine

Ref: 10-F064981