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
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Articles
The Suzuki-Miyaura cross-coupling reaction is an important and extensively used reaction in organic chemistry with applications in polymer science and in the fine chemicals and pharmaceutical industries.
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
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