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CAS 662138-96-7

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N-Phenyldiethanolamine 2-pyridylboronate

Description:
N-Phenyldiethanolamine 2-pyridylboronate is a chemical compound characterized by its unique structure, which includes a phenyl group, diethanolamine moiety, and a boronate group attached to a pyridine ring. This compound typically exhibits properties associated with both amines and boron-containing compounds, making it potentially useful in various applications, including organic synthesis and medicinal chemistry. The presence of the diethanolamine component suggests it may have solubility in polar solvents and could participate in hydrogen bonding interactions. The boronate group is known for its ability to form reversible covalent bonds with diols, which can be advantageous in biochemical applications, such as in the development of sensors or drug delivery systems. Additionally, the pyridine ring may contribute to the compound's electronic properties and reactivity. Overall, N-Phenyldiethanolamine 2-pyridylboronate is a versatile compound with potential applications in research and industry, particularly in fields that leverage its unique chemical functionalities.
Formula:C15H17BN2O2
InChI:InChI=1/C15H17BN2O2/c1-2-6-14(7-3-1)18-10-12-19-16(20-13-11-18)15-8-4-5-9-17-15/h1-9H,10-13H2
SMILES:c1ccc(cc1)N1CCOB(c2ccccn2)OCC1
Synonyms:
  • Pyridine-2-boronic acid N-phenyldiethanolamine ester
  • 6-Phenyl-2-(Pyridin-2-Yl)-1,3,6,2-Dioxazaborocane
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