60137-92-0

Usage

Uses

Used in Liquid Crystal Display (LCD) Industry:
4-ACETYL-4'-PROPYLBIPHENYL is used as a raw material for the production of liquid crystal compounds, which are essential in the manufacturing of liquid crystal displays (LCDs). Its unique properties contribute to the development of high-quality display technologies.
Used in Pharmaceutical Industry:
4-ACETYL-4'-PROPYLBIPHENYL serves as a raw material in the pharmaceutical sector, where it is utilized in the synthesis of various medicinal compounds. Its versatility and stability make it a valuable component in the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical field, 4-ACETYL-4'-PROPYLBIPHENYL is employed as a starting material for the synthesis of agrochemicals, such as pesticides and herbicides. Its properties allow for the creation of effective and stable agricultural products.
Used as an Intermediate in Organic Synthesis:
4-ACETYL-4'-PROPYLBIPHENYL is also used as an intermediate in organic synthesis, where it can be further modified or combined with other compounds to produce a wide range of chemical products for various applications.

Upstream product

• 10289-45-9 4-propyl-1,1'-biphenyl 
• 75-36-5 acetyl chloride 
• 99-90-1 para-bromoacetophenone 
• 134150-01-9 4-propylphenylboric acid 
• 360768-57-6 4-ethenyl-4'-propyl-1,1'-biphenyl 

Relevant academic research and scientific papers

Water-soluble salen-Pd complex as an efficient catalyst for Suzuki-Miyaura reaction of sterically hindered substrates in pure water

Water-soluble 2N2O-salen ligands and their palladium complexes were synthesized and used as efficient catalysts for the Suzuki-Miyaura reactions in pure water. Notably, the reactions of substrates with sterically demanding ortho substituents (aryl bromides and/or arylboronic acids) proceed smoothly to generate corresponding products with moderate to high yields using 0.5 mol % (salph)Pd (salph=N,N′-bis(4-SO3Na-salicylidene)-1,2-phenylenediamine) as the catalyst. Importantly, the catalytic system has the wide substrate scope and the high tolerance to various functional groups, including cyano, amino, nitro, methoxy, and acetyl. Moreover, the biaryl compounds were also obtained on a multi-gram scale by simple recrystallization with the system in the absence of any organic solvent, surfactant, or phase transfer agent and the catalyst was reused directly for the next cycle. Particularly, this protocol can be applied to synthesize aryl-substituted carbazolyl compounds.

Highly efficient AgBF4-catalyzed synthesis of methyl ketones from terminal alkynes

A silver-catalyzed highly efficient synthesis of a wide range of methyl ketones from terminal alkynes is described. The reactions are conducted under convenient conditions and provide products with excellent regioselectivity in moderate to excellent yields, with broad substrate scope, including a variety of aromatic and aliphatic terminal alkynes.