745-36-8

Basic information

• Product Name: 1,1'-Biphenyl, 4-(diphenylmethyl)-
• CAS NO: 745-36-8
• Molecular Formula: C25H20
• Molecular Weight: 320.434
• Mol File: 745-36-8.mol
• Article Data: 14

Chemical Properties

• CAS DataBase Reference: 1,1'-Biphenyl, 4-(diphenylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1'-Biphenyl, 4-(diphenylmethyl)-(745-36-8)
• EPA Substance Registry System: 1,1'-Biphenyl, 4-(diphenylmethyl)-(745-36-8)

Safety Data

• Hazardous Substances Data: 745-36-8(Hazardous Substances Data)

Usage

General Description

1,1'-Biphenyl, 4-(diphenylmethyl)- is a chemical compound that belongs to the category of biphenyl derivatives. It is composed of two benzene rings connected by a single carbon-carbon bond. The substituent group 4-(diphenylmethyl) adds a phenyl group to the fourth carbon atom of one of the benzene rings. 1,1'-Biphenyl, 4-(diphenylmethyl)- is often used in organic synthesis and pharmaceutical research as a building block for more complex molecules, and it possesses various potential applications in the fields of materials science and medicinal chemistry. Additionally, it exhibits interesting properties such as fluorescence and has been studied for its potential use in organic light-emitting diodes (OLEDs) and optoelectronic devices.

Upstream product

• 38696-14-9 4-biphenylyldiphenylmethanol 
• 76-83-5 trityl chloride 
• 109-99-9 tetrahydrofuran 
• 108-86-1 bromobenzene 
• 519-73-3 triphenylmethane 
• 591-50-4 iodobenzene 
• 945-51-7 1,1'-sulfinylbisbenzene 
• 981-18-0 triphenyl(phenylazo)methane 
• 613-31-0 9,10-dihydroanthracene 
• 65864-86-0 phenyl-azo-triphenylmethane 
• 3246-80-8 9-phenyl-9H-xanthene 
• 30905-13-6 4-biphenylylphenyldiazomethane 
• 536-74-3 phenylacetylene 
• 74590-00-4 potassium salt of p-biphenylyldiphenylmethane 

Downstream Products

• 3246-80-8 9-phenyl-9H-xanthene 
• 746-22-5 biphenylyl diphenyl methane cesium salt 
• 67-71-0 dimethylsulfone 
• 67131-60-6 diphenyl methyl anion 
• 536-74-3 phenylacetylene 
• 74590-00-4 potassium salt of p-biphenylyldiphenylmethane 
• 613-31-0 9,10-dihydroanthracene 
• 768-60-5 4-methoxyphenylacetylen 
• 76-84-6 triphenylmethyl alcohol 
• 92-52-4 biphenyl 
• 101-81-5 Diphenylmethane 
• 33240-62-9 4-(Bis-pentachlorophenyl-methyl)-2,3,5,6,2',3',4',5',6'-nonachloro-biphenyl 

Relevant articles and documents

METHOD FOR PRODUCING ARENE COMPOUNDS AND ARENE COMPOUNDS PRODUCED BY THE SAME

Provided is a method for producing (alkyl)arene compounds represented by Formulae 3-1, 3-2, and 3-3 by the Friedel-Crafts alkylation reaction of alkyl halide compounds and arene compounds using organic phosphine compounds as a catalyst.

Synthesis of Di- and Triarylmethanes through Palladium-Catalyzed Reductive Coupling of N -Tosylhydrazones and Aryl Bromides

A palladium-catalyzed reductive coupling between N-tosylhydrazones and aryl bromides has been developed. The reaction provides an efficient method for the synthesis of diarylmethanes and triarylmethanes via the formation of C(sp2)-C(sp3) single bonds. This new methodology for the synthesis of diarylmethanes and triarylmethanes is featured by the ready availability of the starting materials, mild reaction conditions, and the tolerance of wide range of functional groups. The reaction follows a pathway including palladium carbene formation, migratory insertion, and reduction of the alkylpalladium(II) intermediate.

Microwave-assisted nafion-H catalyzed friedel-crafts type reaction of aromatic aldehydes with arenes: Synthesis of triarylmethanes

A new solid acid Nafion-H, a perfluorinated sulfonic acid resin, catalyzed microwave-assisted synthesis of triarylmethanes is described. Various benzaldehydes react readily with arenes to provide the corresponding triarylmethanes in good to excellent yields. The reactions were carried out under solvent free conditions under microwave irradiation in a pressure vessel. The solvent free microwave irradiation methods appears to be an environmentally friendly synthetic protocol providing products in significantly shorter reaction times over traditional heating methods carried out in a pressure tube.