4'-Pentyl-3-fluorobiphenyl-4-boronic acid is an organoboron compound characterized by the presence of a biphenyl structure substituted with a pentyl group and a fluorine atom, along with a boronic acid functional group. This compound typically exhibits properties associated with both organic and inorganic chemistry, including the ability to form complexes with various substrates due to the boronic acid moiety, which can participate in Suzuki coupling reactions. The presence of the pentyl group contributes to its hydrophobic characteristics, while the fluorine atom can influence its electronic properties and reactivity. This compound is often utilized in organic synthesis, particularly in the development of pharmaceuticals and materials science, due to its ability to facilitate cross-coupling reactions. Additionally, the boronic acid group allows for the formation of reversible covalent bonds with diols, making it useful in sensor applications and in the study of biomolecular interactions. Overall, 4'-pentyl-3-fluorobiphenyl-4-boronic acid is a versatile compound with significant applications in various fields of chemistry.

4'-PENTYL-3-FLUOROBIPHENYL-4-BORONIC ACID

163129-14-4: 4'-Pentyl-3-fluorobiphenyl-4-boronic acid is an organoboron compound characterized by the presence of a biphenyl structure substituted with a pentyl group and a fluorine atom, along with a boronic acid functional group. This compound typically exhibits properties associated with both organic and inorganic chemistry, including the ability to form complexes with various substrates due to the boronic acid moiety, which can participate in Suzuki coupling reactions. The presence of the pentyl group contributes to its hydrophobic characteristics, while the fluorine atom can influence its electronic properties and reactivity. This compound is often utilized in organic synthesis, particularly in the development of pharmaceuticals and materials science, due to its ability to facilitate cross-coupling reactions. Additionally, the boronic acid group allows for the formation of reversible covalent bonds with diols, making it useful in sensor applications and in the study of biomolecular interactions. Overall, 4'-pentyl-3-fluorobiphenyl-4-boronic acid is a versatile compound with significant applications in various fields of chemistry.

Boronic acid, B-(3-fluoro-4'-pentyl[1,1'-biphenyl]-4-yl)-

(3-Fluoro-4'-Pentyl-4-Biphenylyl)Boronic Acid

CAS 163129-14-4

4'-PENTYL-3-FLUOROBIPHENYL-4-BORONIC ACID

Boronic acid, B-(3-fluoro-4'-pentyl[1,1'-biphenyl]-4-yl)-

Ref: IN-DA001TSV

(3-Fluoro-4'-Pentyl-4-Biphenylyl)Boronic Acid

Ref: 54-PC104941

(3-Fluoro-4′-pentyl-[1,1′-biphenyl]-4-yl)boronic acid

Ref: 10-F770633