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CAS 1310405-04-9

:

6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2(1H)-pyridinone

Description:
6-(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 reactions such as Suzuki coupling. The compound is likely to exhibit properties typical of both the pyridinone and boron-containing compounds, including potential solubility in organic solvents and the ability to form coordination complexes. Its molecular structure suggests that it may have applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the biological relevance of both the pyridine and boron functionalities. Additionally, the presence of bulky tetramethyl groups may influence its steric properties and reactivity. Overall, this compound represents a versatile building block in synthetic organic chemistry, with potential implications in various fields, including materials science and drug development.
Formula:C11H16BNO3
InChI:InChI=1S/C11H16BNO3/c1-10(2)11(3,4)16-12(15-10)8-6-5-7-9(14)13-8/h5-7H,1-4H3,(H,13,14)
InChI key:InChIKey=MKKJTADNAAPSQP-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C=2NC(=O)C=CC2
Synonyms:
  • 6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2(1H)-pyridinone
  • 2(1H)-Pyridinone, 6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • 6-HYDROXYPYRIDINE-2-BORONIC ACID PINACOL ESTER
  • 6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2(1H)-one
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