29680-44-2

Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 12 carbon (C), 5 hydrogen (H), 1 bromine (Br), and 4 fluorine (F) atoms.

Explanation

Biphenyl is a group of organic compounds consisting of two benzene rings linked together by a single bond. 1,1'-Biphenyl, 4-bromo-2,3,5,6-tetrafluoro- is a specific type of biphenyl with additional bromine and fluorine atoms.
3. Halogenated compound

Explanation

The presence of bromine and fluorine atoms in the compound makes it highly halogenated, which gives it unique chemical and physical properties compared to other biphenyls.

Explanation

Due to its unique properties, 1,1'-Biphenyl, 4-bromo-2,3,5,6-tetrafluoro- is used in various applications, including the synthesis of complex organic molecules, the development of advanced materials and pharmaceuticals, and the production of high-performance polymers.

Explanation

The halogenated nature of 1,1'-Biphenyl, 4-bromo-2,3,5,6-tetrafluoro- may pose potential hazards, so it is crucial to handle it carefully and follow safety guidelines to minimize risks during laboratory work.

Type of compound

Biphenyl

Applications

Organic synthesis, building block for advanced materials and pharmaceuticals, reagent for high-performance polymers, and precursor for other fluorinated compounds

Safety considerations

Handle with care and follow proper safety protocols in a laboratory setting

Upstream product

• 1534-70-9 4-amino-2,3,5,6-tetrafluoro-biphenyl 
• 1559-88-2 1-bromo-2,3,5,6-tetrafluorobenzene 
• 3240-34-4 [bis(acetoxy)iodo]benzene 
• 2996-92-1 phenyl trimethylsiloxane 
• 98-80-6 phenylboronic acid 

Relevant academic research and scientific papers

Novel compound and organic light emitting device comprising the same

The present invention provides a novel compound and an organic light emitting device including the same.

Pd-catalyzed direct arylation of electron-deficient polyfluoroarenes with aryliodine(III) diacetates

A Pd-catalyzed direct arylation of electron-deficient polyfluoroarenes with readily available aryliodine(III) diacetates was developed with moderate to good yields. The process exhibited good functional tolerance with respect to methyl, methoxy, bromo, chloro, trifluoromethyl, cyano, and aldehyde groups. Mechanistic studies revealed this coupling involved in situ generation of aryl iodide from heating-promoted decomposition of aryliodine(III) diacetate, followed by coupling with polyfluoroarenes substrates to afford the desired products.

Palladium-catalyzed direct arylation of polyfluoroarenes with organosilicon reagents

The palladium-catalyzed direct arylation of polyfluoroarenes with organosilicon reagents was achieved by establishing general reaction conditions. This protocol was compatible with a broad range of functional groups and offered the desired products in moderate to good yields. Copyright

Palladium-catalyzed direct arylation of electron-deficient polyfluoroarenes with arylboronic acids

The palladium-catalyzed direct arylation of electron-deficient arenes that contain two or more fluorine groups with arylboronic acids was realized. The key to achieving a broad substrate scope with respect to both polyfluorobenzenes and arylboronic acids