1692-25-7
1692-25-7
Chemical Structure
Pyridin-3-ylboronic acid
- CAS No.: 1692-25-7
- Formula:C5H6BNO2
- Molecular Weight:122.92
IUPAC Name: pyridin-3-ylboronic acid
InChIKey: ABMYEXAYWZJVOV-UHFFFAOYSA-N
SMILES: OB(O)C1=CN=CC=C1
Biological Activity: Pyridin-3-ylboronic acid is a synthetic building block belonging to the pyridine boronic acid class. Pyridin-3-ylboronic acid serves as a substrate for the Suzuki-Miyaura coupling reaction to construct oligopyridine backbones. Pyridin-3-ylboronic acid also acts as a heteroaryl boronic acid in the phosphine-free Suzuki-Miyaura coupling reaction of 2-iodogalactal. Pyridin-3-ylboronic acid is applicable to research related to organic synthesis[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Pyridin-3-ylboronic acid | 98.48% | Pyridin-3-ylboronic acid is a synthetic building block belonging to the pyridine boronic acid class. Pyridin-3-ylboronic acid serves as a substrate for the Suzuki-Miyaura coupling reaction to construct oligopyridine backbones. Pyridin-3-ylboronic acid also acts as a heteroaryl boronic acid in the phosphine-free Suzuki-Miyaura coupling reaction of 2-iodogalactal. Pyridin-3-ylboronic acid is applicable to research related to organic synthesis. | ||||||||||||||||||||
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References
- [1]. Santos JS, et al. Structural characterizations of oligopyridyl foldamers, α-helix mimetics. Journal of chemical information and modeling. 2012 Feb 27;52(2):429-39. [Content Brief]
- [2]. Cobo I, et al. Phosphine-free Suzuki-Miyaura cross-coupling in aqueous media enables access to 2-C-aryl-glycosides. Organic letters. 2012 Apr 06;14(7):1728-31. [Content Brief]
