(3-Bromonaphthalen-2-yl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a naphthalene ring that is substituted with a bromine atom. This compound typically exhibits properties common to boronic acids, such as the ability to form reversible complexes with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the bromine atom enhances its reactivity and can facilitate cross-coupling reactions, such as Suzuki-Miyaura coupling, which is widely used in the formation of carbon-carbon bonds. Additionally, (3-bromonaphthalen-2-yl)boronic acid may exhibit moderate solubility in organic solvents and can participate in further chemical transformations due to the electrophilic nature of the boron atom. Its structural features contribute to its potential utility in the development of pharmaceuticals and advanced materials. As with many organoboron compounds, careful handling and storage are recommended due to their sensitivity to moisture and air.

(3-BROMONAPHTHALEN-2-YL)BORONIC ACID

1301205-62-8: (3-Bromonaphthalen-2-yl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a naphthalene ring that is substituted with a bromine atom. This compound typically exhibits properties common to boronic acids, such as the ability to form reversible complexes with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the bromine atom enhances its reactivity and can facilitate cross-coupling reactions, such as Suzuki-Miyaura coupling, which is widely used in the formation of carbon-carbon bonds. Additionally, (3-bromonaphthalen-2-yl)boronic acid may exhibit moderate solubility in organic solvents and can participate in further chemical transformations due to the electrophilic nature of the boron atom. Its structural features contribute to its potential utility in the development of pharmaceuticals and advanced materials. As with many organoboron compounds, careful handling and storage are recommended due to their sensitivity to moisture and air.

CAS 1301205-62-8

(3-BROMONAPHTHALEN-2-YL)BORONIC ACID

(3-Bromonaphthalen-2-yl)boronic acid

Ref: IN-DA01DV7L

(3-Bromonaphthalen-2-yl)boronic acid

Ref: 54-OR82043

(3-Bromonaphthalen-2-yl)boronic acid

Ref: 10-F758134