512125
3-Pyridinylboronic acid
≥95.0%
Synonym(s):
3-Pyridineboronic acid, 3-Pyridylboronic acid, Dihydroxy(3-pyridyl)borane, Pyridin-3-ylboronic acid
About This Item
Recommended Products
Quality Level
Assay
≥95.0%
form
solid
mp
>300 °C (lit.)
SMILES string
OB(O)c1cccnc1
InChI
1S/C5H6BNO2/c8-6(9)5-2-1-3-7-4-5/h1-4,8-9H
InChI key
ABMYEXAYWZJVOV-UHFFFAOYSA-N
Related Categories
Application
- Phosphine-free Suzuki-Miyaura cross-coupling reactions.
- Regioselective Suzuki-Miyaura coupling and tandem palladium-catalyzed intramolecular aminocarbonylation and annulation.
- N-arylation using copper acetylacetonate catalyst.
- Copper-mediated cyanation and regioselective cyanation of electron-rich benzenes.
It can also be used to prepare:
- New linear poly(phenylpyridyl) chains by Suzuki coupling.
- Oligopyridyl foldamers as mimics of a-helix twist.
- Many highly significant therapeutic enzymatic and kinase inhibitors and receptor antagonists.
- Pyridine substituted pyridinium N-(2′-azinyl)aminides by reacting with dibromo pyridinium aminides via Suzuki coupling reaction.
Other Notes
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
Certificates of Analysis (COA)
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Suzuki-Miyaura cross-coupling reaction is extensively used in organic chemistry, polymer science, and pharmaceutical industries.
Suzuki-Miyaura cross-coupling reaction is extensively used in organic chemistry, polymer science, and pharmaceutical industries.
Suzuki-Miyaura cross-coupling reaction is extensively used in organic chemistry, polymer science, and pharmaceutical industries.
Suzuki-Miyaura cross-coupling reaction is extensively used in organic chemistry, polymer science, and pharmaceutical industries.
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