81793-59-1

Usage

Uses

Used in Organic Chemistry:
4-Fluoro-4'-(4-n-pentylcyclohexyl)biphenyl is used as a building block in the synthesis of various organic compounds. Its versatile structure allows for the creation of a wide range of molecules with different functional groups and properties, making it a valuable component in the development of new organic materials.
Used in Pharmaceutical Research:
4-Fluoro-4'-(4-n-pentylcyclohexyl)biphenyl is studied for its potential pharmacological properties. Researchers are interested in its potential as a pharmaceutical drug or as a chemical intermediate in the production of drugs. Its unique structure may contribute to novel therapeutic effects or improved drug delivery systems.
Used in Materials Science:
In the field of materials science, 4-Fluoro-4'-(4-n-pentylcyclohexyl)biphenyl is of interest for its potential applications in the development of new materials with specific properties. Its unique molecular structure could lead to the creation of materials with enhanced characteristics, such as improved stability, reactivity, or selectivity in various applications.
Used in Chemical Intermediates Production:
4-Fluoro-4'-(4-n-pentylcyclohexyl)biphenyl is also used as a chemical intermediate in the production of other compounds. Its presence in the synthesis process can influence the final product's properties, making it a crucial component in the manufacturing of certain chemicals and pharmaceuticals.

Upstream product

• 1765-93-1 4-fluoroboronic acid 
• 153873-83-7 1-bromo-4-(4-pentylcyclohexyl)benzene 
• 79832-89-6 1-bromo-4-(trans-4-pentylcyclohexyl)benzene 
• 460-00-4 1-Bromo-4-fluorobenzene 

Relevant academic research and scientific papers

An aerobic and very fast Pd/C-catalyzed ligand-free and aqueous Suzuki reaction under mild conditions

An aerobic, ligand-free Suzuki reaction catalyzed by Pd/C in aqueous media has been developed. This method is a very simple, efficient and mild protocol for the cross-coupling of aryl bromides with arylboronic acids, and the reactions proceeded smoothly in excellent yields within short reaction times. Control experiments demonstrated that the Pd/C-catalyzed Suzuki reaction was much quicker when performed in air or oxygen than in nitrogen. Furthermore, this protocol could be used for the synthesis of fluorinated liquid-crystalline compounds. The Pd/C catalyst could be recovered and recycled efficiently at least ten times without significant loss of catalytic activity. Copyright

Metallomicelles of palladium(II) complexes as efficient catalysts for the Suzuki-Miyaura reaction in neat water

Metallomicelles of palladium(II) complex 4 are found to be an efficient catalyst for Suzuki-Miyaura reactions of aryl bromides substituted with a long alkyl chain and arylboronic acids at 80 °C in neat water. The reactions proceed smoothly to generate the corresponding biaryl compounds in moderate to excellent yields. Various biphenyl derivatives were successfully obtained by complex 4 catalysis of the Suzuki-Miyaura reactions in the absence of any surfactants in neat water. Copyright

Salen and half-salen palladium(II) complexes: synthesis, characteriztion and catalytic activity toward Suzuki-Miyaura reaction

Salen and half-salen palladium(II) complexes (salden)Pd (1, salden=N,N′-bis(3,5-di- tert-butylsalicylidene)-1,2-dimethylethylenediamine), (hsalph)PdCl (2, hsalph=3,5-di-tert- butylsalicylidene-1-iminophenylene-2-amine), and (salph)Pd (4, salph=N,N′-bis(3,

Bis(imino)pyridine palladium(II) complexes: Synthesis, structure and catalytic activity

Bis(imino)pyridine palladium(II) complexes 3-6 were synthesized by two different methods. The structure of complexes 3 and 4 has been confirmed by X-ray structure analysis. The catalytic studies show that bis(imino)pyridine palladium(II) complexes are highly efficient catalysts in the Suzuki-Miyaura reaction and the complex 4 was used to catalyze the synthesis of fluorinated liquid crystalline compounds via Suzuki coupling reaction. Crown Copyright

Application of Suzuki cross-coupling reaction catalyzed by ligandless palladium chloride in the synthesis of liquid crystals

Palladium chloride-catalyzed Suzuki cross-coupling reaction was applied to the preparation of highly pure multiring liquid crystals with a biphenyl unit. The optimal reaction condition is the combination of 0.5 mol% PdCl2, pyridine, and K3PO4, which was a