4,9-Dihydro-s-indaceno[1,2-b:5,6-b']dithiophene is an organic compound characterized by its unique fused ring structure, which incorporates both dithiophene and indacene moieties. This compound typically exhibits a planar configuration, contributing to its potential applications in organic electronics, particularly in organic semiconductors and photovoltaic devices. The presence of sulfur atoms in the dithiophene units enhances its electronic properties, allowing for improved charge transport and stability. Additionally, the compound may display interesting optical properties, such as strong absorption in the visible region, making it suitable for light-harvesting applications. Its solubility can vary depending on the substituents attached to the core structure, influencing its processability in various solvents. Overall, 4,9-dihydro-s-indaceno[1,2-b:5,6-b']dithiophene is of significant interest in materials science for its potential use in advanced electronic devices and organic photovoltaics, where its structural characteristics can be leveraged to optimize performance.

4,9-Dihydro-s-indaceno[1,2-b:5,6-b']dithiophene is a yellow solid that can be used in electrochemical devices. It can be used to intensify the color of other molecules and has been shown to have optical properties that are dependent on the moiety. 4,9-Dihydro-s-indaceno[1,2-b:5,6-b']dithiophene is also able to incorporate into chloroform and benzene. It has been shown to form a transfer reaction with anthracene and naphthalene under certain conditions. 4,9-Dihydro-s-indaceno[1,2-b:5,6-b']dithiophene yields a hypsochromic effect in the presence of benzene and naphthalene.

4,9-dihydro-s-indaceno[1,2-b:5,6-b']dithiophene

1209012-31-6: 4,9-Dihydro-s-indaceno[1,2-b:5,6-b']dithiophene is an organic compound characterized by its unique fused ring structure, which incorporates both dithiophene and indacene moieties. This compound typically exhibits a planar configuration, contributing to its potential applications in organic electronics, particularly in organic semiconductors and photovoltaic devices. The presence of sulfur atoms in the dithiophene units enhances its electronic properties, allowing for improved charge transport and stability. Additionally, the compound may display interesting optical properties, such as strong absorption in the visible region, making it suitable for light-harvesting applications. Its solubility can vary depending on the substituents attached to the core structure, influencing its processability in various solvents. Overall, 4,9-dihydro-s-indaceno[1,2-b:5,6-b']dithiophene is of significant interest in materials science for its potential use in advanced electronic devices and organic photovoltaics, where its structural characteristics can be leveraged to optimize performance.

4,9-dihydro-s-indaceno[1,2-b

4,9-Dihydro-s-indaceno[1,2-b:5,6-b']dithiophene

CAS 1209012-31-6

4,9-dihydro-s-indaceno[1,2-b:5,6-b']dithiophene

4,9-dihydro-s-indaceno[1,2-b

Ref: IN-DA0094VQ

4,9-Dihydro-s-indaceno[1,2-b:5,6-b']dithiophene

Ref: 54-OR1039369