214360-45-9

Basic information

• Product Name: 2-(3-Cyanophenyl)-5,5μ-dimethyl-1,3,2-dioxaborinane
• Synonyms: (3-Cyanophenyl)boronic acid, neopentyl glycol ester;2-(3-Cyanophenyl)-5,5μ-dimethyl-1,3,2-dioxaborinane;3-Cyanophenylboronic acid neopentyl ester;3-(5,5-DiMethyl-1,3,2-dioxaborinan-2-yl)benzonitrile;(3-Cyanophenyl)boronic acid, neopentyl glycol ester 95%
• CAS NO: 214360-45-9
• Molecular Formula: C12H14BNO2
• Molecular Weight: 215.06
• Mol File: 214360-45-9.mol
• Article Data: 3

Chemical Properties

• Melting Point: 85-87 °C
• Boiling Point: 350.2°C at 760 mmHg
• Flash Point: 165.6°C
• Appearance: /
• Density: 1.08g/cm³
• Vapor Pressure: 4.48E-05mmHg at 25°C
• Refractive Index: 1.511
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 2-(3-Cyanophenyl)-5,5μ-dimethyl-1,3,2-dioxaborinane(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3-Cyanophenyl)-5,5μ-dimethyl-1,3,2-dioxaborinane(214360-45-9)
• EPA Substance Registry System: 2-(3-Cyanophenyl)-5,5μ-dimethyl-1,3,2-dioxaborinane(214360-45-9)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• WGK Germany: 3
• Hazardous Substances Data: 214360-45-9(Hazardous Substances Data)

Usage

Uses

(3-Cyanophenyl)boronic acid, neopentyl glycol ester

InChI:InChI=1/C12H14BNO2/c1-12(2)8-15-13(16-9-12)11-5-3-4-10(6-11)7-14/h3-6H,8-9H2,1-2H3

Upstream product

• 126-30-7 2,2-Dimethyl-1,3-propanediol 
• 150255-96-2 (3‐cyanophenyl)boronic acid 

Downstream Products

• 13531-48-1 methyl 3-cyanobenzoate 
• 886570-18-9 3-(2-nitrobenzyl)benzonitrile 
• 400748-29-0 3'-formyl-[1,1'-biphenyl]-3-carbonitrile 

Relevant articles and documents

Nickel-Catalyzed Regioselective Alkenylarylation of γ,δ-Alkenyl Ketones via Carbonyl Coordination

We disclose a nickel-catalyzed reaction, which enabled us to difunctionalize unactivated γ,δ-alkenes in ketones with alkenyl triflates and arylboronic esters. The reaction was made feasible by the use of 5-chloro-8-hydroxyquinoline as a ligand along with

Cu-Catalyzed cross-coupling reactions of epoxides with organoboron compounds

A copper-catalyzed cross-coupling reaction of epoxides with arylboronates is described. This reaction is not limited to aromatic epoxides, because aliphatic epoxides are also suitable substrates. In addition, N-sulfonyl aziridines can be successfully converted into the products. This reaction provides convenient access to β-phenethyl alcohols, which are valuable synthetic intermediates.