2,8-Diiododibenzothiophene is an organic compound characterized by its structure, which features a dibenzothiophene backbone with two iodine substituents at the 2 and 8 positions. This compound is notable for its potential applications in organic electronics, particularly in organic semiconductors and photovoltaic devices, due to its conjugated system that allows for effective charge transport. The presence of iodine atoms enhances its electronic properties and can influence its solubility and reactivity. Additionally, dibenzothiophene derivatives are of interest in materials science for their photophysical properties, which can be tuned through substitution. The compound is typically synthesized through halogenation reactions and may exhibit distinct physical properties such as color and melting point, influenced by the presence of the iodine atoms. As with many organoiodine compounds, it may also exhibit unique reactivity patterns, making it a subject of interest in synthetic organic chemistry. Safety and handling precautions should be observed due to the potential toxicity associated with iodine-containing compounds.

2,8-Diiododibenzothiophene

105404-91-9: 2,8-Diiododibenzothiophene is an organic compound characterized by its structure, which features a dibenzothiophene backbone with two iodine substituents at the 2 and 8 positions. This compound is notable for its potential applications in organic electronics, particularly in organic semiconductors and photovoltaic devices, due to its conjugated system that allows for effective charge transport. The presence of iodine atoms enhances its electronic properties and can influence its solubility and reactivity. Additionally, dibenzothiophene derivatives are of interest in materials science for their photophysical properties, which can be tuned through substitution. The compound is typically synthesized through halogenation reactions and may exhibit distinct physical properties such as color and melting point, influenced by the presence of the iodine atoms. As with many organoiodine compounds, it may also exhibit unique reactivity patterns, making it a subject of interest in synthetic organic chemistry. Safety and handling precautions should be observed due to the potential toxicity associated with iodine-containing compounds.

CAS 105404-91-9

2,8-Diiododibenzothiophene

2,8-Diiododibenzothiophene

Ref: 3B-D4870

2,8-Diiododibenzothiophene

Ref: IN-DA008Y12

2,8-Diiododibenzothiophene

Ref: 54-OR1010211