For research use only. Not for therapeutic Use.
2-(2-Cyanophenyl)-1,3,2-dioxaborinane (Cat No.: R021403) is an organoboron compound featuring a six-membered dioxaborinane ring attached to a 2-cyanophenyl group. This structure combines the reactivity of boronic esters with the electron-withdrawing effects of a nitrile group, making it valuable in cross-coupling reactions such as Suzuki–Miyaura coupling. It serves as a stable boron-containing intermediate for synthesizing biaryl and heteroaryl compounds, often used in pharmaceutical and materials research. Its cyclic boronate structure also offers enhanced stability and handling over traditional boronic acids.
CAS Number | 172732-52-4 |
Synonyms | 2-(1,3,2-Dioxaborinan-2-yl)benzonitrile; |
Molecular Formula | C10H10BNO2 |
Purity | ≥95% |
Storage | -20°C |
IUPAC Name | 2-(1,3,2-dioxaborinan-2-yl)benzonitrile |
InChI | InChI=1S/C10H10BNO2/c12-8-9-4-1-2-5-10(9)11-13-6-3-7-14-11/h1-2,4-5H,3,6-7H2 |
InChIKey | REQZFVYFYAZUMG-UHFFFAOYSA-N |
SMILES | B1(OCCCO1)C2=CC=CC=C2C#N |
Chemistry Calculators | Dilution Calculator In vivo Formulation Calculator Molarity Calculator Molecular Weight Calculator Reconstitution Calculator |