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CAS 286961-15-7

:

Phenylmethyl 3,6-dihydro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1(2H)-pyridinecarboxylate

Description:
Phenylmethyl 3,6-dihydro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1(2H)-pyridinecarboxylate, identified by its CAS number 286961-15-7, is a chemical compound that features a pyridine ring substituted with a carboxylate group and a boron-containing moiety. This compound is characterized by its complex structure, which includes a dihydropyridine framework and a boron-dioxaborolane unit, contributing to its potential reactivity and applications in organic synthesis. The presence of the boron atom suggests that it may participate in various chemical reactions, such as cross-coupling reactions, making it of interest in medicinal chemistry and materials science. Additionally, the tetramethyl groups enhance its stability and solubility in organic solvents. The compound's unique structural features may also impart specific biological activities, warranting further investigation into its pharmacological properties. Overall, this compound exemplifies the intersection of organic chemistry and materials science, with potential applications in drug development and synthetic methodologies.
Formula:C19H26BNO4
InChI:InChI=1S/C19H26BNO4/c1-18(2)19(3,4)25-20(24-18)16-10-12-21(13-11-16)17(22)23-14-15-8-6-5-7-9-15/h5-10H,11-14H2,1-4H3
InChI key:InChIKey=QDSFHRPYZPQWEJ-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C=2CCN(C(OCC3=CC=CC=C3)=O)CC2
Synonyms:
  • 1(2H)-Pyridinecarboxylic acid, 3,6-dihydro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, phenylmethyl ester
  • 4-(4,4,5,5-Tetramethyl-[1,3,2]Dioxaborolan-2-Yl)-3,6-Dihydro-2H-Pyridine-1-Carboxylic Acid Benzyl Ester
  • Benzyl 3,6-dihydro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-pyridine-1-carboxylate
  • Benzyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydropyridine-1(2H)-carboxylate
  • Phenylmethyl 3,6-dihydro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1(2H)-pyridinecarboxylate
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