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CAS 848093-29-8

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5-Formylpyridine-3-boronic acid pinacol ester

Description:
5-Formylpyridine-3-boronic acid pinacol ester is an organoboron compound characterized by the presence of a pyridine ring, a formyl group, and a boronic acid moiety esterified with pinacol. This compound typically exhibits a white to off-white solid appearance and is soluble in organic solvents such as dichloromethane and ethanol. The presence of the boronic acid functionality allows for participation in various chemical reactions, particularly in Suzuki coupling reactions, which are essential for forming carbon-carbon bonds in organic synthesis. The formyl group provides a reactive aldehyde site, making it useful in further functionalization or as an intermediate in synthetic pathways. Additionally, the pinacol ester group enhances the stability of the boronic acid, making it easier to handle and store. Overall, 5-Formylpyridine-3-boronic acid pinacol ester is a valuable compound in medicinal chemistry and materials science, facilitating the development of complex organic molecules.
Formula:C12H16BNO3
InChI:InChI=1S/C12H16BNO3/c1-11(2)12(3,4)17-13(16-11)10-5-9(8-15)6-14-7-10/h5-8H,1-4H3
SMILES:CC1(C)C(C)(C)OB(c2cc(cnc2)C=O)O1
Synonyms:
  • 5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinaldehyde
  • 5-FORMYLPYRIDINE-3-BORONIC ACID PINACOL ESTER
  • 3-hydroxy-2,3-dimethylbutan-2-yl hydrogen (5-formylpyridin-3-yl)boronate
  • 5-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-PYRIDINE-3-CARBALDEHYDE
  • 5-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-3-carbaldehyde
  • ne
  • 5-Formyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
  • 5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinaldehyde, 5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine-3-carboxaldehyde, 3-Formyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridi
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