864059-66-5

Basic information

• Product Name: 2,3-Difluoro-4'-methyl-1,1'-Biphenyl
• Synonyms: 2,3-Difluoro-4'-methyl-1,1'-Biphenyl;2,3-Difluoro-4'-Methylbiphenyl
• CAS NO: 864059-66-5
• Molecular Formula: C13H10F2
• Molecular Weight: 204
• Mol File: 864059-66-5.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 270.9 °C at 760 mmHg
• Flash Point: 97.3 °C
• Appearance: /
• Density: 1.138 g/cm³
• CAS DataBase Reference: 2,3-Difluoro-4'-methyl-1,1'-Biphenyl(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-Difluoro-4'-methyl-1,1'-Biphenyl(864059-66-5)
• EPA Substance Registry System: 2,3-Difluoro-4'-methyl-1,1'-Biphenyl(864059-66-5)

Safety Data

• Hazardous Substances Data: 864059-66-5(Hazardous Substances Data)

Usage

General Description

2,3-Difluoro-4'-methyl-1,1'-Biphenyl is a chemical compound with the molecular formula C13H9F2. It consists of a biphenyl core with two fluorine atoms at the 2 and 3 positions and a methyl group at the 4' position. 2,3-Difluoro-4'-methyl-1,1'-Biphenyl is used in organic synthesis and can be utilized as a building block in the preparation of various pharmaceuticals, agrochemicals, and materials. It has potential applications in the field of organic electronics and optoelectronic devices due to its unique molecular structure and electronic properties. Additionally, it may also be used as a research tool in the study of organic chemistry and material science.

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Relevant articles and documents

Iron-catalyzed coupling of aryl sulfamates and aryl/vinyl tosylates with aryl grignards

The iron-catalyzed coupling of aryl sulfamates and tosylates with aryl Grignard reagents is reported for the first time. The methodology employs air-stable, low-cost FeF3·3H2O and the N-heterocyclic carbene ligand IPr·HCl as the preligand to form a long-lived catalyst upon treatment with aryl Grignards. The reaction provides a range of cross-coupled products in good-to-excellent yields. In contrast to previous reports with aryl chlorides, these reactions proceed with low levels of Grignard homocoupling regardless of the iron source.

Catalytic intermolecular direct arylation of perfluorobenzenes

Penta-, tetra-, tri-, and difluorobenzenes undergo direct arylation with a wide range of arylhalides in high yield. Inverse reactivity is observed compared to the common electrophilic aromatic substitution pathway since electron-deficient, C-H acidic aren

Process for the preparation of 2,3-difluorobenzenes

1,4-disubstituted 2,3-difluorobenzenes according to formula I are suitable as intermediates for the synthesis of liquid crystalline compounds.