5-Mercapto-4-phenyl-3H-1,2-dithiole-3-thione, with the CAS number 16101-90-9, is a heterocyclic compound characterized by its unique sulfur-containing structure. This compound features a dithiole ring, which is a five-membered ring containing two sulfur atoms and three carbon atoms, along with a phenyl group that enhances its aromatic properties. The presence of a thiol (-SH) group contributes to its reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and redox processes. Its thione functionality indicates that it can exist in tautomeric forms, which may influence its chemical behavior and stability. This compound has garnered interest in organic synthesis and materials science due to its potential applications in the development of organic semiconductors and as a ligand in coordination chemistry. Additionally, its unique structure may impart interesting biological activities, warranting further investigation into its pharmacological properties. Overall, 5-mercapto-4-phenyl-3H-1,2-dithiole-3-thione is a versatile compound with significant implications in both synthetic and applied chemistry.

5-MERCAPTO-4-PHENYL-3H-1,2-DITHIOLE-3-THIONE

16101-90-9: 5-Mercapto-4-phenyl-3H-1,2-dithiole-3-thione, with the CAS number 16101-90-9, is a heterocyclic compound characterized by its unique sulfur-containing structure. This compound features a dithiole ring, which is a five-membered ring containing two sulfur atoms and three carbon atoms, along with a phenyl group that enhances its aromatic properties. The presence of a thiol (-SH) group contributes to its reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and redox processes. Its thione functionality indicates that it can exist in tautomeric forms, which may influence its chemical behavior and stability. This compound has garnered interest in organic synthesis and materials science due to its potential applications in the development of organic semiconductors and as a ligand in coordination chemistry. Additionally, its unique structure may impart interesting biological activities, warranting further investigation into its pharmacological properties. Overall, 5-mercapto-4-phenyl-3H-1,2-dithiole-3-thione is a versatile compound with significant implications in both synthetic and applied chemistry.

CAS 16101-90-9

5-MERCAPTO-4-PHENYL-3H-1,2-DITHIOLE-3-THIONE

3H-1,2-Dithiole-3-thione, 5-mercapto-4-phenyl-

Ref: IN-DA001VLE

4-Phenyl-5-thio-3H-1,2-dithiole-3-thione

Ref: 54-OR30153