10270-27-6

Basic information

• Product Name: 4-(2-phenylethyl)benzonitrile
• CAS NO: 10270-27-6
• Molecular Formula: C₁₅H₁₃N
• Molecular Weight: 207.2704
• Mol File: 10270-27-6.mol
• Article Data: 26

Chemical Properties

• Boiling Point: 331.7°C at 760 mmHg
• Flash Point: 155°C
• Density: 1.07g/cm³
• Vapor Pressure: 0.000154mmHg at 25°C
• Refractive Index: 1.591
• CAS DataBase Reference: 4-(2-phenylethyl)benzonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(2-phenylethyl)benzonitrile(10270-27-6)
• EPA Substance Registry System: 4-(2-phenylethyl)benzonitrile(10270-27-6)

Safety Data

• Hazardous Substances Data: 10270-27-6(Hazardous Substances Data)

Upstream product

• 623-00-7 4-bromobenzenecarbonitrile 
• 108-86-1 bromobenzene 
• 69395-13-7 4-(2-hydroxyethyl)benzonitrile 
• 100-39-0 benzyl bromide 
• 17201-43-3 4-cyanobenzyl bromide 
• 3058-39-7 4-iodobenzonitrile 
• 17376-04-4 2-phenethyl iodide 
• 114-84-1 phenylpropionic acid sodium salt 
• 100-42-5 styrene 
• 67753-90-6 B-2-phenylethyl-9-BBN 
• 26104-68-7 (p-cyanobenzyl)triphenylphosphonium bromide 
• 100-51-6 benzyl alcohol 
• 1565829-30-2 phenethyl MIDA boronate 
• 1425503-22-5 4-(2-benzyl-1,3-dithian-2-yl)benzonitrile 

Relevant articles and documents

Preparation of Alkyl Indium Reagents by Iodine-Catalyzed Direct Indium Insertion and Their Applications in Cross-Coupling Reactions

An efficient method for the synthesis of alkyl indium reagent by means of an iodine-catalyzed direct indium insertion into alkyl iodide in THF is reported. The thus-generated alkyl indium reagents effectively underwent Pd-catalyzed cross-coupling reactions with various aryl halides, exhibiting good compatibility to a variety of sensitive functional groups. By replacing THF with DMA and using 0.75 equiv of iodine, less reactive alkyl bromide could be used as substrate for indium insertion with equal ease.

Cesium carbonate-catalyzed indium insertion into alkyl iodides and their synthetic utilities in cross-coupling reactions

A catalytic amount of cesium carbonate (10?mol%) was found to be capable of effectively catalyzing the insertion of indium powder into alkyl iodides. The thus-generated alkyl indium reagents could readily undergo palladium-catalyzed cross-coupling reactions with a wide variety of aryl halides, showing compatibility to a range of important functional groups.

Cobalt(II)-catalyzed preparation of alkylindium reagents and applications in cross-coupling with aryl halides

The direct insertion of indium powder into alkyl iodides was found to be efficiently catalyzed by a catalytic amount of cobalt(II) bromide (10 mol%). Upon subjection of the thus-formed alkylindium compounds to palladium-catalyzed cross-coupling reactions with a wide range of aryl halides, a series of cross-coupled products could be obtained in moderate to good yields with the tolerance to many important functional groups.

Photoredox Heterobimetallic Dual Catalysis Using Engineered Covalent Organic Frameworks

The functionalization of an imine-based layered covalent organic framework (COF), containing phenanthroline units as ligands, has allowed the obtention of a heterobimetallated material. Photoactive Ir and Ni fragments were immobilized within the porous structure of the COF, enabling heterogeneous light-mediated Csp3-Csp2cross-couplings. As radical precursors, potassium benzyl- and alkoxy-trifluoroborates, organic silicates, and proline derivatives were employed, which brings out the good versatility ofIr,Ni@Phen-COF. Moreover, in all the studied cases, an enhanced activity and stability have been observed in comparison with analogous homogenous systems.

Photo-catalytic preparation method of bibenzyl compounds

The invention relates to a preparation method of bibenzyl compounds. A compound represented by a formula (A) and a compound represented by a formula (C) carry out reactions under the action of an organic tungsten catalyst and an alkali in the presence of light to generate bibenzyl compounds represented by the formula (B). The method is simple and is easy to operate. The yield is high, and the application range is wide. Moreover, the invention also provides an application of a tungsten complex in organic chemical reactions as a photocatalyst.