6-Bromo-1,2,3,4-tetrahydro-2-naphthalenol is an organic compound characterized by its bicyclic structure, which includes a naphthalene core modified by a hydroxyl group and a bromine atom. This compound features a tetrahydro configuration, indicating that it has undergone partial hydrogenation, resulting in a saturated ring system. The presence of the bromine substituent introduces notable reactivity, making it a potential candidate for various chemical transformations, including nucleophilic substitutions and coupling reactions. The hydroxyl group contributes to its polarity, enhancing its solubility in polar solvents and influencing its interactions in biological systems. This compound may exhibit interesting pharmacological properties, as many naphthalene derivatives are known for their biological activity. Additionally, its structural features suggest potential applications in organic synthesis and materials science. As with many brominated compounds, considerations regarding environmental impact and toxicity are essential, particularly in terms of persistence and bioaccumulation. Overall, 6-bromo-1,2,3,4-tetrahydro-2-naphthalenol represents a versatile structure in organic chemistry with implications in both research and application.

6-BROMO-1,2,3,4-TETRAHYDRO-2-NAPHTHALENOL

173996-27-5: 6-Bromo-1,2,3,4-tetrahydro-2-naphthalenol is an organic compound characterized by its bicyclic structure, which includes a naphthalene core modified by a hydroxyl group and a bromine atom. This compound features a tetrahydro configuration, indicating that it has undergone partial hydrogenation, resulting in a saturated ring system. The presence of the bromine substituent introduces notable reactivity, making it a potential candidate for various chemical transformations, including nucleophilic substitutions and coupling reactions. The hydroxyl group contributes to its polarity, enhancing its solubility in polar solvents and influencing its interactions in biological systems. This compound may exhibit interesting pharmacological properties, as many naphthalene derivatives are known for their biological activity. Additionally, its structural features suggest potential applications in organic synthesis and materials science. As with many brominated compounds, considerations regarding environmental impact and toxicity are essential, particularly in terms of persistence and bioaccumulation. Overall, 6-bromo-1,2,3,4-tetrahydro-2-naphthalenol represents a versatile structure in organic chemistry with implications in both research and application.

CAS 173996-27-5

6-BROMO-1,2,3,4-TETRAHYDRO-2-NAPHTHALENOL

2-Naphthalenol, 6-bromo-1,2,3,4-tetrahydro-

Ref: IN-DA001ZC6

6-Bromo-1,2,3,4-tetrahydronaphthalen-2-ol

Ref: 10-F640423

6-Bromo-1,2,3,4-tetrahydronaphthalen-2-ol

Ref: 3D-YGA99627