89346-54-3

Basic information

• Product Name: 2'-BROMO-4-FLUORO-BIPHENYL
• Synonyms: 2'-BROMO-4-FLUORO-BIPHENYL;1,1'-Biphenyl, 2-broMo-4'-fluoro-
• CAS NO: 89346-54-3
• Molecular Formula: C₁₂H₈BrF
• Molecular Weight: 251.0943232
• Mol File: 89346-54-3.mol
• Article Data: 22

Chemical Properties

• Appearance: /
• Density: 1.433±0.06 g/cm3 (20 ºC 760 Torr)
• CAS DataBase Reference: 2'-BROMO-4-FLUORO-BIPHENYL(CAS DataBase Reference)
• NIST Chemistry Reference: 2'-BROMO-4-FLUORO-BIPHENYL(89346-54-3)
• EPA Substance Registry System: 2'-BROMO-4-FLUORO-BIPHENYL(89346-54-3)

Safety Data

• Hazardous Substances Data: 89346-54-3(Hazardous Substances Data)

Usage

General Description

2'-Bromo-4-fluoro-biphenyl is a chemical compound with the molecular formula C12H8BrF. It is a derivative of biphenyl that contains a bromine and a fluorine atom attached to the aromatic rings. 2'-BROMO-4-FLUORO-BIPHENYL is mainly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It is also used as a building block in organic chemistry and can be utilized in the production of liquid crystals and OLED materials. Additionally, 2'-bromo-4-fluoro-biphenyl has potential applications in the field of materials science and organic electronics due to its unique electronic and optical properties. However, it is important to handle this compound with care, as it can be harmful if ingested or inhaled, and may cause skin and eye irritation upon contact. Please note that the provided information is for reference purposes only and is not intended to be used as a basis for purchasing or using this product. It is important to consult with a qualified professional or reference the specific safety data sheet for handling and usage guidelines.

Upstream product

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Downstream Products

• 179526-94-4 (4'-fluoro-[1,1'-biphenyl]-2-yl)boronic acid 
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Relevant articles and documents

Rhodium-Catalyzed Synthesis of Chiral Monohydrosilanes by Intramolecular C?H Functionalization of Dihydrosilanes

The preparation of chiral monohydrosilanes remains a rarely achieved goal. To this end a Rh-catalyzed desymmetrization of dihydrosilanes by way of intramolecular C(sp2)?H functionalization under simple and mild conditions has now been developed

Synthesis of Dibenzosiloles through Electrocatalytic Sila-Friedel-Crafts Reaction

A novel electrocatalyzed method for the preparation of dibenzosiloles was developed through intramolecular C?H/Si?H dehydrogenative coupling strategy starting from biarylhydrosilanes. Both electro-donating and electro-withdrawing substitution groups were tolerated for this transformation, and the desired dibenzosilole products could be obtained in moderate to excellent yields. A sila-Friedel-Crafts reaction mechanism was proposed on the basis of previous literature and our controlled experiments. (Figure presented.).

Ag-Catalyzed Cyclization of Arylboronic Acids with Elemental Selenium for the Synthesis of Selenaheterocycles

A general method for the synthesis of five-membered and six-membered selenaheterocycles through Ag-catalyzed C?Se bond-forming reaction is reported. This reaction proceeds via intramolecular cyclization of arylboronic acids with selenium powder. Preliminary mechanism studies demonstrate that this transformation involves a selenium-centred radical intermediate. (Figure presented.).