1423-26-3
1423-26-3
Chemical Structure
3-(Trifluoromethyl)phenylboronic acid
- CAS No.: 1423-26-3
- Formula:C7H6BF3O2
- Molecular Weight:189.93
IUPAC Name: (3-(trifluoromethyl)phenyl)boronic acid
InChIKey: WOAORAPRPVIATR-UHFFFAOYSA-N
SMILES: FC(C1=CC(B(O)O)=CC=C1)(F)F
Biological Activity: 3-(Trifluoromethyl)phenylboronic acid usually undergoes linear selective hydroarylation reaction with alkenes as a substrate[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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3-(Trifluoromethyl)phenylboronic acid | 99.81% | 3-(Trifluoromethyl)phenylboronic acid usually undergoes linear selective hydroarylation reaction with alkenes as a substrate. | ||||||||||||||||||||
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References
- [1]. Liu C C, et al. Expanding the C1‐Symmetric Bicyclo [2.2. 1] heptadiene Ligand Family: Highly Enantioselective Synthesis of Cyclic β‐Aryl‐Substituted Carbonyl Compounds[J]. European Journal of Organic Chemistry, 2012, 2012(13): 2503-2507.
- [2]. Lv H, et al. Nickel(0)-catalyzed linear-selective hydroarylation of unactivated alkenes and styrenes with aryl boronic acids. Chem Sci. 2018 Jul 18;9(33):6839-6843. [Content Brief]
