CAS 4612-26-4

1,4-Benzenediboronic acid

Description:

1,4-Benzenediboronic acid, with the CAS number 4612-26-4, is an organic compound characterized by the presence of two boronic acid functional groups attached to a benzene ring at the 1 and 4 positions. This compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and alcohols. It is known for its ability to form stable complexes with diols, making it useful in various applications, including organic synthesis and materials science. The boronic acid groups can participate in Suzuki coupling reactions, which are valuable in the formation of carbon-carbon bonds in organic chemistry. Additionally, 1,4-benzenediboronic acid can serve as a building block in the synthesis of polymers and other complex molecules. Its reactivity and functional versatility make it an important compound in the development of pharmaceuticals and advanced materials. Safety precautions should be observed when handling this compound, as with many boron-containing substances, due to potential irritant properties.

Formula: C₆H₈B₂O₄

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

SMILES: c1cc(ccc1B(O)O)B(O)O

Synonyms:

• 1,4-Phenylenediboronic acid
• 4-(Dihydroxyboryl)phenylboronic acid
• 1,4-Phenylenebisboronic acid
• Benzene-1,4-diboronic acid
• 1,4-Phenylenebis(Boronic Acid)
• P-Phenylenediboronic Acid
• 1,4-Phenyldiboronic acid
• Benzene-1,4-Diyldiboronic Acid

1,4-Phenylenediboronic Acid (contains varying amounts of Anhydride)

CAS: 4612-26-4

Formula: C₆H₈B₂O₄

Color and Shape: White to Light yellow to Light orange powder to crystal

Molecular weight: 165.75

Ref: 3B-P1358

1,4-Benzenediboronic acid, 96%

CAS: 4612-26-4

It is used for palladium-catalyzed sequential alkenylation and conjugate addition reactions, scholl cyclizations, Suzuki-Miyaura cross-coupling reactions. It is also used in the preparation of indolizine derivatives as OLEDs, in organic thin-film transistors, Fluorescence and solution-processable co

Formula: C₆H₈B₂O₄

Purity: 96%

Color and Shape: White to pale cream, Powder

Molecular weight: 165.75

Ref: 02-B24064

1,4-Phenylenediboronic acid

CAS: 4612-26-4

Formula: C₆H₈B₂O₄

Purity: 97%

Color and Shape: Solid

Molecular weight: 165.7473

Ref: IN-DA0032N6

1,4-Benzenediboronic acid

CAS: 4612-26-4

Formula: C₆H₈B₂O₄

Purity: 97.0 - 112.0 %

Color and Shape: White to off-white solid

Molecular weight: 165.75

Ref: 7W-GK4896

Benzene-1,4-diboronic acid

CAS: 4612-26-4

Benzene-1,4-diboronic acid

Formula: C₆H₈B₂O₄

Purity: 97%

Color and Shape: white to off-white solid

Molecular weight: 165.75g/mol

Ref: 54-OR7148

1,4-Phenylenediboronic acid

CAS: 4612-26-4

Formula: C₆H₈B₂O₄

Purity: 97%

Color and Shape: Solid, Powder or Crystalline Powder or or Solid or Chunks

Molecular weight: 165.75

Ref: 10-F045301

1,4-Phenylenebisboronic acid

CAS: 4612-26-4

1,4-Phenylenebisboronic acid is a chemical compound with the following structural formula:
It is a white crystalline solid, soluble in water and ethanol. 1,4-Phenylenebisboronic acid has been used for analytical chemistry and photochemical studies. It has also been studied as a model system for ternary complex formation, x-ray diffraction data analysis, and ester linkages. Structural analysis of 1,4-phenylenebisboronic acid reveals hydrogen bonding interactions between the nitrogen atoms and the boron atoms.

Formula: C₆H₈B₂O₄

Purity: Min. 95 Area-%

Color and Shape: Powder

Molecular weight: 165.75 g/mol

Ref: 3D-FP74696