3-Bromodibenzothiophene is an organic compound characterized by its structure, which consists of a dibenzothiophene core with a bromine substituent at the 3-position. This compound features a fused ring system that includes both sulfur and aromatic carbon rings, contributing to its unique chemical properties. It is typically a solid at room temperature and may exhibit a range of colors depending on its purity and specific form. The presence of the bromine atom introduces halogen characteristics, which can influence its reactivity, solubility, and potential applications in organic synthesis and materials science. 3-Bromodibenzothiophene may also exhibit interesting electronic properties due to its conjugated system, making it a candidate for use in organic electronics, such as organic semiconductors or photovoltaic devices. Additionally, its sulfur content may impart specific chemical reactivity, allowing for further functionalization or derivatization in synthetic chemistry. As with many organic compounds, safety precautions should be observed when handling this substance, as it may pose health risks or environmental hazards.

3-Bromodibenzothiophene

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3-Bromodibenzo[b,d]thiophene

3-Bromodibenzothiophene is a synthetic, carboxylate ligand that can be used as a catalyst to promote cross-coupling reactions with ethylene. This compound has been shown to be photocyclized in the presence of UV light and emits luminescence. 3-Bromodibenzothiophene also has carcinogenic properties and is classified as hazardous for human health.

CAS 97511-04-1: 3-Bromodibenzothiophene

3-Bromodibenzo[b,d]thiophene

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3-Bromodibenzo[b,d]thiophene

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3-Bromodibenzothiophene

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3-Bromodibenzothiophene

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3-Bromodibenzothiophene

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