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CAS 181219-01-2

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Pyridine-4-boronic acid pinacol cyclic ester

Description:
Pyridine-4-boronic acid pinacol cyclic ester, with the CAS number 181219-01-2, is a boronic acid derivative characterized by its unique structure that includes a pyridine ring and a boronic acid functional group. This compound typically exhibits properties such as being a white to off-white solid, soluble in polar organic solvents, and possessing a moderate melting point. The presence of the boronic acid moiety allows it to participate in various chemical reactions, particularly in Suzuki coupling reactions, making it valuable in organic synthesis and medicinal chemistry. The cyclic ester formation enhances its stability and reactivity, facilitating its use in the development of pharmaceuticals and agrochemicals. Additionally, this compound may exhibit moderate to low toxicity, and appropriate safety measures should be taken when handling it in laboratory settings. Overall, pyridine-4-boronic acid pinacol cyclic ester is an important building block in synthetic organic chemistry, contributing to the advancement of various chemical applications.
Formula:C11H18BNO3
InChI:InChI=1/C11H16BNO2/c1-10(2)11(3,4)15-12(14-10)9-5-7-13-8-6-9/h5-8H,1-4H3
SMILES:CC1(C)C(C)(C)OB(c2ccncc2)O1
Synonyms:
  • 2-(4-Pyridyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
  • 4-Pyridylboronic acid pinacol ester
  • 4-Pyridineboronic acid pinacol ester
  • Pyridine-4-boronic acid pinacol ester
  • PYRIDIN-4-YLBORONIC ACID, PINACOL ESTER
  • 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine, 4-Pyridylboronic acid pinacol ester
  • 4-Pyridineboronic acid, pinacol cyclic ester
  • PYRIDINE-4-BORONIC PINACOLATE
  • AKOS BRN-0440
  • See more synonyms
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