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5,6-Dihydro-4H-cyclopenta-1,2-dithiole-3-thione, with the CAS number 14085-33-7, is a heterocyclic compound characterized by its unique bicyclic structure that incorporates sulfur atoms. This compound features a cyclopentadiene-like framework fused with two sulfur atoms, contributing to its distinct chemical properties. It is known for its potential applications in organic synthesis and materials science, particularly in the development of organic semiconductors and photovoltaic materials. The presence of the thione functional group enhances its reactivity, allowing it to participate in various chemical reactions, including nucleophilic substitutions and cycloadditions. Additionally, this compound exhibits interesting electronic properties due to the conjugation within its structure, which can influence its behavior in different chemical environments. Its stability and solubility can vary depending on the solvent and conditions used, making it a subject of interest in both academic and industrial research. Overall, 5,6-dihydro-4H-cyclopenta-1,2-dithiole-3-thione is a versatile compound with significant potential in various fields of chemistry.

5,6-DIHYDRO-4H-CYCLOPENTA-1,2-DITHIOLE-3-THIONE

14085-33-7: 5,6-Dihydro-4H-cyclopenta-1,2-dithiole-3-thione, with the CAS number 14085-33-7, is a heterocyclic compound characterized by its unique bicyclic structure that incorporates sulfur atoms. This compound features a cyclopentadiene-like framework fused with two sulfur atoms, contributing to its distinct chemical properties. It is known for its potential applications in organic synthesis and materials science, particularly in the development of organic semiconductors and photovoltaic materials. The presence of the thione functional group enhances its reactivity, allowing it to participate in various chemical reactions, including nucleophilic substitutions and cycloadditions. Additionally, this compound exhibits interesting electronic properties due to the conjugation within its structure, which can influence its behavior in different chemical environments. Its stability and solubility can vary depending on the solvent and conditions used, making it a subject of interest in both academic and industrial research. Overall, 5,6-dihydro-4H-cyclopenta-1,2-dithiole-3-thione is a versatile compound with significant potential in various fields of chemistry.

CPDT is an orally active and potent inducer of phase 2 enzymes as well as an activator of Nrf2. CPDT enhances the activity of critical phase 2 enzymes, such as glutathione S-transferase, NAD(P)H:quinone oxidoreductase 1, and gamma-glutamylcysteine synthetase, and increases glutathione levels both in the bladder of rats and in bladder cells in vitro.

CAS 14085-33-7

5,6-DIHYDRO-4H-CYCLOPENTA-1,2-DITHIOLE-3-THIONE

CPDT

Ref: TM-T204763

Cyclopenta[c]-1,2-dithiole-3(4H)-thione, 5,6-dihydro-

Ref: IN-DA001CWZ