3-Bromo-4-iodothiophene is a heterocyclic organic compound characterized by its thiophene ring, which is a five-membered aromatic ring containing sulfur. The presence of bromine and iodine substituents at the 3 and 4 positions, respectively, introduces significant reactivity and influences its electronic properties. This compound typically exhibits a yellow to brown color and is soluble in organic solvents such as dichloromethane and chloroform, but may have limited solubility in water. Its molecular structure contributes to its potential applications in organic electronics, such as in the development of semiconductors and photovoltaic materials. Additionally, the halogen substituents can facilitate further chemical modifications, making it a versatile intermediate in synthetic organic chemistry. The compound's reactivity is also influenced by the electron-withdrawing nature of the halogens, which can affect its behavior in various chemical reactions, including nucleophilic substitutions and coupling reactions. Safety precautions should be taken when handling this compound, as it may pose health risks due to the presence of halogens.

3-Bromo-4-iodothiophene

73882-41-4: 3-Bromo-4-iodothiophene is a heterocyclic organic compound characterized by its thiophene ring, which is a five-membered aromatic ring containing sulfur. The presence of bromine and iodine substituents at the 3 and 4 positions, respectively, introduces significant reactivity and influences its electronic properties. This compound typically exhibits a yellow to brown color and is soluble in organic solvents such as dichloromethane and chloroform, but may have limited solubility in water. Its molecular structure contributes to its potential applications in organic electronics, such as in the development of semiconductors and photovoltaic materials. Additionally, the halogen substituents can facilitate further chemical modifications, making it a versatile intermediate in synthetic organic chemistry. The compound's reactivity is also influenced by the electron-withdrawing nature of the halogens, which can affect its behavior in various chemical reactions, including nucleophilic substitutions and coupling reactions. Safety precautions should be taken when handling this compound, as it may pose health risks due to the presence of halogens.

CAS 73882-41-4

3-Bromo-4-iodothiophene

3-Bromo-4-iodothiophene

Ref: IN-DA005ALK

3-Bromo-4-iodothiophene

Ref: 10-F232158