2-Bromo-4,5,6,7-tetrahydro-1-benzothiophene is a heterocyclic organic compound characterized by its unique bicyclic structure that incorporates both a benzene ring and a thiophene ring. The presence of a bromine atom at the 2-position enhances its reactivity, making it useful in various chemical syntheses and applications. This compound typically exhibits a pale yellow to brownish color and is soluble in organic solvents. Its molecular structure contributes to its potential biological activity, which has been explored in medicinal chemistry. The tetrahydro configuration indicates that the compound has undergone partial hydrogenation, resulting in a saturated ring system that can influence its physical and chemical properties, such as boiling point and stability. Additionally, the compound's reactivity can be attributed to the electron-withdrawing nature of the bromine atom, which can facilitate nucleophilic substitution reactions. Overall, 2-bromo-4,5,6,7-tetrahydro-1-benzothiophene is of interest in both synthetic organic chemistry and pharmacological research.

2-BroMo-4,5,6,7-tetrahydro-1-benzothiophene

111873-07-5: 2-Bromo-4,5,6,7-tetrahydro-1-benzothiophene is a heterocyclic organic compound characterized by its unique bicyclic structure that incorporates both a benzene ring and a thiophene ring. The presence of a bromine atom at the 2-position enhances its reactivity, making it useful in various chemical syntheses and applications. This compound typically exhibits a pale yellow to brownish color and is soluble in organic solvents. Its molecular structure contributes to its potential biological activity, which has been explored in medicinal chemistry. The tetrahydro configuration indicates that the compound has undergone partial hydrogenation, resulting in a saturated ring system that can influence its physical and chemical properties, such as boiling point and stability. Additionally, the compound's reactivity can be attributed to the electron-withdrawing nature of the bromine atom, which can facilitate nucleophilic substitution reactions. Overall, 2-bromo-4,5,6,7-tetrahydro-1-benzothiophene is of interest in both synthetic organic chemistry and pharmacological research.

2-Bromo-4,5,6,7-tetrahydro-1-benzothiophene

2-Bromo-4,5,6,7-tetrahydrobenzo[b]thiophene

CAS 111873-07-5

2-BroMo-4,5,6,7-tetrahydro-1-benzothiophene

2-Bromo-4,5,6,7-tetrahydro-1-benzothiophene

Ref: IN-DA009440

2-Bromo-4,5,6,7-tetrahydrobenzo[b]thiophene

Ref: 54-OR61152

2-Bromo-4,5,6,7-tetrahydrobenzo[b]thiophene

Ref: 10-F459666