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CAS 159191-44-3

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4-(DIBENZYLAMINO)PHENYLBORONIC ACID

Description:
4-(Dibenzylamino)phenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a dibenzylamino group. This compound typically exhibits properties such as being a white to off-white solid, with moderate solubility in organic solvents and limited solubility in water due to its hydrophobic dibenzylamino moiety. It is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis, medicinal chemistry, and as a reagent in the development of sensors. The presence of the boronic acid group allows for participation in Suzuki-Miyaura cross-coupling reactions, which are pivotal in constructing complex organic molecules. Additionally, this compound may exhibit biological activity, making it of interest in pharmaceutical research. Safety data should be consulted for handling, as boronic acids can be irritants and require appropriate safety measures during use.
Formula:C20H20BNO2
InChI:InChI=1/C20H20BNO2/c23-21(24)19-11-13-20(14-12-19)22(15-17-7-3-1-4-8-17)16-18-9-5-2-6-10-18/h1-14,23-24H,15-16H2
SMILES:c1ccc(cc1)CN(Cc1ccccc1)c1ccc(cc1)B(O)O
Synonyms:
  • 4-(N,N-Dibenzylamino)Phenylboronic Acid
  • 4-(Dibenzylamino)benzeneboronic acid
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