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CAS 321724-19-0

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Pyrimidine-5-boronic acid pinacol ester

Description:
Pyrimidine-5-boronic acid pinacol ester is an organoboron compound characterized by the presence of a pyrimidine ring and a boronic acid functional group, which is esterified with pinacol. This compound typically exhibits properties common to boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various organic synthesis applications, particularly in the formation of carbon-carbon bonds through Suzuki coupling reactions. The pyrimidine moiety contributes to its potential biological activity and solubility characteristics. Generally, boronic esters are stable under neutral conditions but can hydrolyze in the presence of water or under acidic or basic conditions. Pyrimidine-5-boronic acid pinacol ester may also exhibit fluorescence properties, depending on its specific structure and substituents. Its applications span medicinal chemistry, materials science, and organic synthesis, where it serves as a versatile building block for more complex molecules. Safety data should be consulted for handling and storage, as with all chemical substances.
Formula:C10H15BN2O2
InChI:InChI=1/C10H15BN2O2/c1-9(2)10(3,4)15-11(14-9)8-5-12-7-13-6-8/h5-7H,1-4H3
SMILES:CC1(C)C(C)(C)OB(c2cncnc2)O1
Synonyms:
  • Pyrimidine, 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • 5-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Pyrimidine
  • Pinacol Ester Pyrimidinyl-5-Boronic Acid
  • 5-(Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Pyrimidine
  • PYRIMIDYL-5-BORONIC ACID PINACOLATE
  • PYRIMIDINE-5-BORONIC ACID PINACOL ESTER
  • PYRIMIDYL-5-BORONIC ACID PINACOL ESTER
  • PYRIMIDINE-5-BORONIC ACID PINACOLATE
  • AKOS BRN-1136
  • PYRIMIDIN-5-YLBORONIC ACID PINACOL ESTER
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