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CAS 1073354-99-0

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5-Aminopyridine-3-boronicacid,pinacolester

Description:
5-Aminopyridine-3-boronic acid pinacol ester is an organoboron compound characterized by the presence of both an amino group and a boronic acid moiety, which is esterified with pinacol. This compound typically exhibits properties associated with boron-containing compounds, such as the ability to form reversible covalent bonds with diols and other nucleophiles, making it useful in various chemical reactions, including Suzuki coupling reactions. The amino group contributes to its potential as a ligand in coordination chemistry and may enhance its solubility in polar solvents. Additionally, the presence of the pyridine ring imparts aromatic characteristics, influencing its electronic properties and reactivity. This compound is often utilized in organic synthesis, medicinal chemistry, and materials science due to its versatile reactivity and ability to participate in cross-coupling reactions. Safety data should be consulted for handling, as organoboron compounds can have specific hazards associated with their use.
Formula:C11H17BN2O2
InChI:InChI=1S/C11H17BN2O2/c1-10(2)11(3,4)16-12(15-10)8-5-9(13)7-14-6-8/h5-7H,13H2,1-4H3
InChI key:InChIKey=DAISWHFZWZZBBD-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C=2C=C(N)C=NC2
Synonyms:
  • 3-Aminopyrdine-5-boronic acid pinacol ester
  • 3-Pyridinamine, 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • 5-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Pyridin-3-Amine
  • 5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinamine
  • 5-Aminopyridine-3-Boronic Acid Pinacol Ester
  • [5-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)pyridin-3-yl]amine
  • (5-AMINOPYRIDIN-3-YL)BORONIC ACID PINACOL ESTER
  • 2-yl)-pyridin-3-ylamine
  • 5-AMINOPYRIDINE-3-BORONIC ACID, PICOL ESTER
  • 3-AMinopyridin-5-ylboronic acid pinacol ester
  • See more synonyms
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