6-Bromohexylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group and a bromoalkyl chain. Its molecular structure includes a six-carbon hexyl chain with a bromine atom attached to the sixth carbon, along with a boronic acid group (-B(OH)2) that is known for its ability to form reversible covalent bonds with diols, making it useful in various chemical reactions, particularly in Suzuki coupling reactions. This compound is typically a white to off-white solid and is soluble in polar solvents such as water and alcohols, which enhances its utility in organic synthesis and medicinal chemistry. The presence of the bromine atom provides a site for nucleophilic substitution reactions, while the boronic acid functionality allows for the formation of boronate esters. 6-Bromohexylboronic acid is often employed in the development of pharmaceuticals and agrochemicals, as well as in materials science for the synthesis of polymers and other complex structures. Safety precautions should be observed when handling this compound due to its reactive nature.

6-Bromohexylboronic acid

148562-12-3: 6-Bromohexylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group and a bromoalkyl chain. Its molecular structure includes a six-carbon hexyl chain with a bromine atom attached to the sixth carbon, along with a boronic acid group (-B(OH)2) that is known for its ability to form reversible covalent bonds with diols, making it useful in various chemical reactions, particularly in Suzuki coupling reactions. This compound is typically a white to off-white solid and is soluble in polar solvents such as water and alcohols, which enhances its utility in organic synthesis and medicinal chemistry. The presence of the bromine atom provides a site for nucleophilic substitution reactions, while the boronic acid functionality allows for the formation of boronate esters. 6-Bromohexylboronic acid is often employed in the development of pharmaceuticals and agrochemicals, as well as in materials science for the synthesis of polymers and other complex structures. Safety precautions should be observed when handling this compound due to its reactive nature.

CAS 148562-12-3

6-Bromohexylboronic acid

Boronic acid, B-(6-bromohexyl)-

Ref: IN-DA001L0D

6-Bromohexylboronic acid

Ref: 54-OR360360

(6-Bromohexyl)boronic acid

Ref: 10-F696351