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CAS 957198-31-1

:

2-(1-Piperazinyl)pyridine-4-boronic acid pinacol ester

Description:
2-(1-Piperazinyl)pyridine-4-boronic acid pinacol ester is a chemical compound characterized by its boronic acid functionality, which is often utilized in medicinal chemistry and organic synthesis. The presence of the piperazine moiety suggests potential biological activity, as piperazine derivatives are known for their pharmacological properties. The pyridine ring contributes to the compound's aromatic character and may influence its electronic properties and reactivity. The pinacol ester group enhances the stability of the boronic acid, making it more suitable for various applications, including cross-coupling reactions in organic synthesis. This compound is likely to be a white to off-white solid, soluble in polar organic solvents, and may exhibit moderate to high stability under standard laboratory conditions. Its unique structure allows for potential interactions with biological targets, making it of interest in drug discovery and development. As with many boronic acids, it may also participate in reversible covalent bonding with diols, which is a key feature in the design of sensors and other functional materials.
Formula:C15H24BN3O2
InChI:InChI=1/C15H24BN3O2/c1-14(2)15(3,4)21-16(20-14)12-5-6-18-13(11-12)19-9-7-17-8-10-19/h5-6,11,17H,7-10H2,1-4H3
SMILES:CC1(C)C(C)(C)OB(c2ccnc(c2)N2CCNCC2)O1
Synonyms:
  • 2-(1-Piperazino)pyridine-4-boronic acid pinacol ester, 97%
  • 1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-2-yl)piperazine
  • 2-(Piperazin-1-yl)pyridine-4-boronic acid
  • (2-(PIPERAZIN-1-YL)PYRIDIN-4-YL)BORONIC ACID PINACOL ESTER
  • 2-(Piperazin-1-yl)pyridine-4-boronic acid, picol ester
  • 2-(1-Piperazinyl)pyridine-4-boronic acid pinacol ester 97%
  • Piperazine, 1-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-pyridinyl]-
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