7418-16-8

Usage

Uses

Used in Automotive Industry:
2,2-BIS(4-OXOCYCLOHEXYL)PROPANE is used as a key ingredient in the production of high-temperature resistant coatings and adhesives for automotive applications, ensuring durability and performance under demanding conditions.
Used in Aerospace Industry:
In the aerospace sector, 2,2-BIS(4-OXOCYCLOHEXYL)PROPANE serves as a critical component in the development of coatings and adhesives that can withstand the extreme temperatures and harsh chemical environments encountered in space and high-altitude flight.
Used in Industrial Manufacturing:
2,2-BIS(4-OXOCYCLOHEXYL)PROPANE is utilized as a fundamental material in the creation of coatings and adhesives for various industrial manufacturing processes, providing robust protection and bonding capabilities in high-stress and high-temperature environments.

Upstream product

• 13804-54-1 4,4'-isopropylidenedicyclohexanol 
• 80-05-7 BPA 
• 64-19-7 acetic acid 

Downstream Products

• 13804-62-1 C₁₉H₃₆O₄ 

Relevant academic research and scientific papers

The cyclohexanone derivative

[Problem] to the cyclohexanone derivative, which can be efficiently manufactured at a low cost in a safe method. One or more of the hydroxy groups in one or more of benzene and 1 2 [a] having 6 - 30 carbon atoms in the raw material compound, in the presence of a hydrogenation catalyst in a solvent by, one or more of cyclohexanone derivative comprises one or more ketone structure 1 has a structure in which cyclohexanone 2 method, cyclohexanone is used as a solvent containing an alcohol derivative. [Drawing] no

Ruthenium-on-Carbon-Catalyzed Facile Solvent-Free Oxidation of Alcohols: Efficient Progress under Solid-Solid (Liquid)-Gas Conditions

A protocol for the ruthenium-on-carbon (Ru/C)-catalyzed solvent-free oxidation of alcohols, which proceeds efficiently under solid-solid (liquid)-gas conditions, was developed. Various primary and secondary alcohols were transformed to corresponding aldehydes and ketones in moderate to excellent isolated yields by simply stirring in the presence of 10% Ru/C under air or oxygen conditions. The solvent-free oxidation reactions proceeded efficiently regardless of the solid or liquid state of the substrates and reagents and could be applied to gram-scale synthesis without loss of the reaction efficiency. Furthermore, the catalytic activity of Ru/C was maintained after five reuse cycles.

Process for producing alicyclic monoketones and process for producing alicyclic diketones

The process for producing alicyclic monoketones (hydroxyphenylcyclohexanone derivatives) according to the present invention comprises hydrogenating substituted bisphenols such as bisphenol A in a solvent in the presence of a palladium/alkali metal catalyst in which palladium and an alkali metal are both supported on a carrier to obtain alicyclic monoketones such as 2-(4-oxocyclohexyl)-2-(4-hydroxyphenyl)propane. The process for producing alicyclic diketones according to the present invention comprises hydrogenating substituted bisphenols such as bisphenol A in a solvent in the presence of a palladium/alkali metal catalyst in which palladium and an alkali metal are both supported on a carrier to obtain alicyclic diketones such as 2,2-bis(4-oxocyclohexyl)propane and 4,4′-bicyclohexanone. The other process for producing alicyclic monoketones according to the present invention comprises hydrogenating biphenols such as bis(4-hydroxyphenyl) in an organic solvent in the presence of a palladium catalyst in which 10 to 30% by weight of palladium is supported on a carrier to obtain alicyclic monoketones such as 4(4′-hydroxyphenyl)cyclohexanone. According to the present invention, alicyclic monoketones or alicyclic diketones can be obtained with high selectivity and in high yields through simple steps, because the process includes only one reaction step to hydrogenate substituted bisphenols under relatively mild conditions.