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CAS 1256358-90-3

:

4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2(1H)-pyridinone

Description:
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2(1H)-pyridinone is a chemical compound characterized by its unique structure, which includes a pyridinone moiety and a dioxaborolane group. The presence of the dioxaborolane ring contributes to its potential reactivity, particularly in organoboron chemistry, where it can participate in various coupling reactions. The compound is likely to exhibit properties typical of both the pyridinone and boron-containing compounds, such as potential coordination with metal ions and involvement in nucleophilic substitution reactions. Its tetramethyl substitution enhances its steric bulk, which may influence its solubility and reactivity. Additionally, the compound may have applications in medicinal chemistry or materials science, given the importance of boron-containing compounds in drug development and organic synthesis. As with many boron compounds, it may also exhibit interesting optical properties or serve as a precursor for further chemical modifications. Safety and handling precautions should be observed, as with all chemical substances, due to potential reactivity and toxicity.
Formula:C11H16BNO3
InChI:InChI=1S/C11H16BNO3/c1-10(2)11(3,4)16-12(15-10)8-5-6-13-9(14)7-8/h5-7H,1-4H3,(H,13,14)
InChI key:InChIKey=UQTTXNHBLCIRLA-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CC(=O)NC=C2
Synonyms:
  • 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-ol
  • 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2(1H)-pyridinone
  • 2(1H)-Pyridinone, 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • 2-Hydroxypyridine-4-boronic acid pinacol ester
  • 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyridin-2-one
  • 4-(4,4,5,5-TetraMethyl-1,3,2-dioxaborolan-2-yl)pyridin-2(1H)-one
  • 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-ol, 2-Hydroxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
  • 2-(Hydroxy)pyridine-4-boronic acid picol ester
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