Substance
ID:319564
Names and Identifiers
IUPAC name
(pyridin-3-yl)boronic acid
IUPAC Traditional name
pyridin-3-ylboronic acid
Synonyms
3-Pyridylboronic acid吡啶-3-硼酸Dihydroxy(3-pyridyl)boranePyridin-3-ylboronic acid3-Pyridinylboronic acid3-Pyridineboronic acid3-吡啶硼酸
Properties
Physical Property
Melting Point
>300 °C(lit.)
Product Information
Empirical Formula (Hill Notation)
C5H6BNO2
Purity
≥95.0%
Safety Information
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
MSDS Link
German water hazard class
3
Molecule Details
Other Notes
Contains varying amounts of anhydride
Packaging
1, 5, 25 g in glass bottle
Application
Reagent used for
• Phosphine-free Suzuki-Miyaura cross-coupling reactions1
• Regioselective Suzuki-Miyaura coupling and tandem palladium-catalyzed intramolecular aminocarbonylation and annulation2
• N-arylation using copper acetylacetonate catalyst3
• Copper-mediated cyanation and regioselective cyanation of electron-rich benzenes4 Reagent use in Preparation of
• New linear poly(phenylpyridyl) chains by Suzuki coupling5
• Oligopyridyl foldamers as mimics of a-helix twist6
• Many highly significant therapeutic enzymatic and kinase inhibitors and receptor antagonists7,8,9
Contains varying amounts of anhydride
Packaging
1, 5, 25 g in glass bottle
Application
Reagent used for
• Phosphine-free Suzuki-Miyaura cross-coupling reactions1
• Regioselective Suzuki-Miyaura coupling and tandem palladium-catalyzed intramolecular aminocarbonylation and annulation2
• N-arylation using copper acetylacetonate catalyst3
• Copper-mediated cyanation and regioselective cyanation of electron-rich benzenes4 Reagent use in Preparation of
• New linear poly(phenylpyridyl) chains by Suzuki coupling5
• Oligopyridyl foldamers as mimics of a-helix twist6
• Many highly significant therapeutic enzymatic and kinase inhibitors and receptor antagonists7,8,9
Molecular Spectra
No Data Available
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References
No Data Available
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