32316-92-0
32316-92-0
Chemical Structure
2-Naphthylboronic acid
- CAS No.: 32316-92-0
- Formula:C10H9BO2
- Molecular Weight:171.99
IUPAC Name: Naphthalen-2-boronic acid
InChIKey: KPTRDYONBVUWPD-UHFFFAOYSA-N
SMILES: OB(O)C1=CC2=CC=CC=C2C=C1
Biological Activity: 2-Naphthylboronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. 2-Naphthylboronic acid can undergo silylation reaction. 2-Naphthylboronic acid also readily undergo Suzuki-Miyaura cross-coupling[1][2].
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2-Naphthylboronic acid | 99.96% | 2-Naphthylboronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. 2-Naphthylboronic acid can undergo silylation reaction. 2-Naphthylboronic acid also readily undergo Suzuki-Miyaura cross-coupling. | ||||||||||||||||||||
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2-Naphthylboronic acid-d7 | 96.13% | 2-Naphthylboronic acid-d7 is the deuterium labeled 2-Naphthylboronic acid (HY-W002570). 2-Naphthylboronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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References
- [1]. Ihara, H., et al., (2009). Easily attachable and detachable ortho-directing agent for arylboronic acids in ruthenium-catalyzed aromatic C-H silylation. Journal of the American Chemical Society, 131(22), 7502–7503. [Content Brief]
- [2]. Victor G. Bardakov, et al., (2022) Organoboron Derivatives of 1,8-Bis(dimethylamino)naphthalene: Synthesis, Structure, Stability, and Reactivity. Organometallics 2022, 41, 12, 1501–1508.
