5-Bromo-2,1,3-benzothiadiazole is a heterocyclic compound characterized by its unique structure, which includes a benzothiadiazole core with a bromine substituent at the 5-position. This compound is typically a solid at room temperature and exhibits a yellow to orange color. It is known for its applications in organic electronics, particularly in the development of organic semiconductors and photovoltaic materials due to its electron-accepting properties. The presence of the bromine atom enhances its reactivity and solubility in various organic solvents, making it useful in synthetic chemistry. Additionally, 5-bromo-2,1,3-benzothiadiazole can participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, which are valuable in the synthesis of more complex organic molecules. Its stability and relatively low toxicity make it a candidate for further research in materials science and medicinal chemistry. Overall, this compound is significant in both academic research and potential industrial applications.

5-bromo-2,1,3-benzothiadiazole

1753-75-9: 5-Bromo-2,1,3-benzothiadiazole is a heterocyclic compound characterized by its unique structure, which includes a benzothiadiazole core with a bromine substituent at the 5-position. This compound is typically a solid at room temperature and exhibits a yellow to orange color. It is known for its applications in organic electronics, particularly in the development of organic semiconductors and photovoltaic materials due to its electron-accepting properties. The presence of the bromine atom enhances its reactivity and solubility in various organic solvents, making it useful in synthetic chemistry. Additionally, 5-bromo-2,1,3-benzothiadiazole can participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, which are valuable in the synthesis of more complex organic molecules. Its stability and relatively low toxicity make it a candidate for further research in materials science and medicinal chemistry. Overall, this compound is significant in both academic research and potential industrial applications.

CAS 1753-75-9

5-bromo-2,1,3-benzothiadiazole

5-Bromobenzo-2,1,3-thiadiazole

Ref: IN-DA0020WR

5-Bromo-2,1,3-benzothiadiazole

Ref: 54-OR23131

5-Bromo-benzo[2,1,3]thiadiazole

Ref: 10-F070498