CAS 4612-28-6: 1,3-Benzenediboronic acid

Description: 1,3-Benzenediboronic acid, with the CAS number 4612-28-6, is an organic compound characterized by the presence of two boronic acid functional groups attached to a benzene ring at the 1 and 3 positions. This compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and alcohols. Its structure allows it to participate in various chemical reactions, particularly in the formation of boronate esters, which are useful in organic synthesis and materials science. 1,3-Benzenediboronic acid is often employed in cross-coupling reactions, such as Suzuki-Miyaura coupling, to form carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules. Additionally, it can act as a ligand in coordination chemistry and has applications in the development of sensors and drug delivery systems due to its ability to form reversible complexes with diols. Its reactivity and versatility make it an important compound in both academic research and industrial applications.

Formula: C₆H₈B₂O₄

InChI: InChI=1/C6H8B2O4/c9-7(10)5-2-1-3-6(4-5)8(11)12/h1-4,9-12H

Synonyms:

• 1,3-Phenylenediboronic acid
• Benzene-1,3-Diyldiboronic Acid

1,3-Benzenediboronic Acid

CAS: 4612-28-6

• Formula: C₆H₈B₂O₄
• Purity: 97%
• Color and Shape: Solid
• Molecular weight: 165.7473

1,3-Benzenediboronic acid

CAS: 4612-28-6

• Formula: C₆H₈B₂O₄
• Molecular weight: 165.75

1,3-Phenylenediboronic acid

CAS: 4612-28-6

• Formula: C₆H₈B₂O₄
• Purity: 98%
• Color and Shape: white solid
• Molecular weight: 165.75g/mol

1,3-Phenylenediboronic acid

CAS: 4612-28-6

• Purity: 97.0%
• Color and Shape: Solid, White to off-white crystalline solid
• Molecular weight: 165.75

1,3-Benzenediboronicacid

CAS: 4612-28-6

1,3-Benzenediboronic acid is a boric acid that has optical properties and can be used in …

• Formula: C₆H₈B₂O₄
• Purity: Min. 95%
• Molecular weight: 165.75 g/mol