3- (Trifluoromethyl) phenylboronic acid

3- (Trifluoromethyl) phenylboronic acid usually undergoes linear selective hydroarylation reaction with alkenes as a substrate[1][2].

Product Specifications

CAS Number

[1423-26-3]

UNSPSC

12352200

Hazard Statement

H302, H315, H319, H335

Target

Biochemical Assay Reagents

Type

Biochemical Assay Reagents

Related Pathways

Others

Field of Research

Others

Assay Protocol

https://www.medchemexpress.com/3-trifluoromethyl-phenylboronic-acid.html

Purity

99.94

Solubility

DMSO : ≥ 100 mg/mL

Smiles

FC(C1=CC(B(O)O)=CC=C1)(F)F

Molecular Formula

C7H6BF3O2

Molecular Weight

189.93

Precautions

H302, H315, H319, H335

References & Citations

[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.