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CAS 13506-83-7

:

B,B′-1,2-Phenylenebis[boronic acid]

Description:
B,B′-1,2-Phenylenebis[boronic acid], with the CAS number 13506-83-7, is an organoboron compound characterized by the presence of two boronic acid functional groups attached to a phenylene backbone. This compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and alcohols due to the presence of the boronic acid groups, which can form hydrogen bonds. It exhibits properties that make it useful in various applications, particularly in organic synthesis and materials science, where it can act as a building block for the formation of complex organic structures. The boronic acid moieties allow for reversible covalent bonding with diols, making it valuable in the development of sensors and drug delivery systems. Additionally, B,B′-1,2-Phenylenebis[boronic acid] can participate in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is significant in the synthesis of pharmaceuticals and agrochemicals. Its reactivity and functional versatility make it an important compound in both academic research and industrial applications.
Formula:C6H8B2O4
InChI:InChI=1S/C6H8B2O4/c9-7(10)5-3-1-2-4-6(5)8(11)12/h1-4,9-12H
InChI key:InChIKey=ZKRVXVDQQOVOIM-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(B(O)O)C=CC=C1
Synonyms:
  • Boronic acid, B,B′-1,2-phenylenebis-
  • 1,2-Phenylenediboronic acid
  • B,B′-1,2-Phenylenebis[boronic acid]
  • o-Benzenediboronic acid
  • Boronic acid, 1,2-phenylenebis-
  • (2-boronophenyl)boronic acid
  • 1,2-phenylenebisboronic acid
  • BORONIC ACID, 1,2-PHENYLENEBIS-BORONIC ACID
  • Boronic acid, 1,2-phenylenebis- (9CI)
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