31516-55-9

Usage

Uses

Used in Pharmaceutical Industry:
2,4-Diphenyl-2-methylpentane is used as a building block in the synthesis of various organic compounds for pharmaceutical applications. Its high purity and stability contribute to the development of new drugs and medicinal products.
Used in Industrial Applications:
In the industrial sector, 2,4-Diphenyl-2-methylpentane serves as a versatile compound for the synthesis of different organic compounds, contributing to the production of various materials and products.
Used in Research and Development:
2,4-Diphenyl-2-methylpentane is utilized as a key component in the research and development of new materials and products. Its unique properties and reactivity make it a valuable asset in scientific exploration and innovation.
It is crucial to handle 2,4-Diphenyl-2-methylpentane with care and adhere to proper safety precautions to minimize potential hazards associated with its use.

Upstream product

• 22768-22-5 4-methyl-2,4-diphenylpent-2-ene 
• 7403-42-1 4-Methyl-4-phenyl-2-pentanone 
• 98-83-9 isopropenylbenzene 
• 6362-80-7 2,4-diphenyl-4-methyl-pent-1-ene 

Downstream Products

• 98-82-8 Isopropylbenzene 
• 1985-57-5 2-methyl-2-phenylpentane 
• 2613-76-5 1,3,3-trimethylindane 
• 100-41-4 ethylbenzene 
• 71-43-2 benzene 
• 696-29-7 (1-methylethyl)-cyclohexane 
• 98-83-9 isopropenylbenzene 

Relevant academic research and scientific papers

Ambient Hydrogenation and Deuteration of Alkenes Using a Nanostructured Ni-Core–Shell Catalyst

A general protocol for the selective hydrogenation and deuteration of a variety of alkenes is presented. Key to success for these reactions is the use of a specific nickel-graphitic shell-based core–shell-structured catalyst, which is conveniently prepared by impregnation and subsequent calcination of nickel nitrate on carbon at 450 °C under argon. Applying this nanostructured catalyst, both terminal and internal alkenes, which are of industrial and commercial importance, were selectively hydrogenated and deuterated at ambient conditions (room temperature, using 1 bar hydrogen or 1 bar deuterium), giving access to the corresponding alkanes and deuterium-labeled alkanes in good to excellent yields. The synthetic utility and practicability of this Ni-based hydrogenation protocol is demonstrated by gram-scale reactions as well as efficient catalyst recycling experiments.

Polysilane-supported transition metal catalyst for liquid phase reaction

The present invention provides a polysilane-supported transition metal catalysts or a polysilane/inorganic compound-supported transition metal catalysts, wherein various types of transition metals are supported by polysilane compounds, or combination of polysilanes and inorganic compounds. The catalysts of the present invention are hardly soluble in hydrocarbons and alcohols and are useful as catalysts in heterogeneous system for various organic synthetic reactions using the above solvents. Polysilanes supporting transition metals are easily crosslinkable by thermal treatment, microwave irradiation, UV irradiation or chemical methods such as hydrosilylation reaction and are changed to be insoluble in various solvents keeping high catalytic activity. Moreover, the stability and operability of polysilane-supported transition metal catalysts will be improved by the support thereof on inorganic compounds. These polysilane-supported transition metal catalysts show a high catalytic activity in hydrogenation reaction, hydrosilylation reaction, Heck reaction, Suzuki-Miyaura coupling reactions and the like. The catalyst is easily recoverable and reusable and the leakage of metals is extremely few.

Development of microchannel reactors using polysilane-supported palladium catalytic systems in capillaries

A new method of immobilizing Pd catalysts on the channel wall of a capillary by using polysilane with metal oxide has been developed, and applied to hydrogenation reactions. The Royal Society of Chemistry.

Practical access to the polymer incarcerated platinum (PI Pt) catalyst and its application to hydrogenation

Polymer incarcerated platinum catalysts (PI Pt) were conveniently prepared from PtCl2(COD) or H2PtCl6·6H 2O and styrene copolymers via reduction of the Pt sources with triethylamine, coacervation, and cross-linking. The Pt catalysts have been successfully applied to catalytic hydrogenation including saturation of heterocyclic compounds. The Royal Society of Chemistry 2006.

METHOD OF CATALYTIC REACTION USING MICRO-REACTOR

A method of catalytic reaction uses a micro-reactor (1) with a metal catalyst (5) or a metal complex catalyst (5) as a solid phase supported on the inner wall (4c) of a channel (4), a solution (7) dissolving a reactant as a liquid phase and hydrogen (9) as a gas phase are flown through the channel (4) in pipe flow state, and the reaction of the solution (7) and the gas (9) accelerated by the metal catalyst (5) or the metal complex catalyst (5) is conducted by three phase catalytic reaction of solid - liquid - gas phases. The metal catalyst (5) or the metal complex catalyst (5) is incorporated in a polymer, and hydrogenation reaction by three phase catalytic reductive reaction of a substance to be reduced can be conducted in short time at good yield. For hydrogenation reaction of unsaturated organics, the rate of reaction and yield are high when palladium catalyst is used, and carbonylation reaction can be conducted if carbon monoxide is used instead of hydrogen.

Polysilane-supported Pd and Pt nanoparticles as efficient catalysts for organic synthesis

Polysilane-supported Pd and Pt catalysts have been prepared for the first time, and used successfully in hydrogenation, Suzuki and Sonogashira reactions, and hydrosilylation respectively: the reactions proceeded in high yields, and the catalysts could be recovered almost quantitatively by simple filtration and reused. The Royal Society of Chemistry 2006.

Hydrogenation reactions using scCO2 as a solvent in microchannel reactors

We have developed an effective microfluidic system for hydrogenation reactions in ScCO2; the reactions proceeded very rapidly (within 1 second), by making the best use of ScCO2 and utilizing the large specific interfacial area of the microchannel reactor, and high reaction productivity was attained in each channel. The Royal Society of Chemistry 2005.

Recoverable, Reusable, Highly Active, and Sulfur-Tolerant Polymer Incarcerated Palladium for Hydrogenation

A new type of immobilized palladium, PI (polymer incarcerated) Pd (2b), from Pd(PPh3)4 and copolymer (1b) has been developed. The excellent activity of PI Pd has been demonstrated in hydrogenation of various olefins, benzyl ethers, and nitro and aromatic compounds. PI Pd is tolerant under high pressure and high temperature and can be recovered and reused several times without loss of activity even under harsh conditions. Moreover, PI Pd is highly resistant to poisoning by sulfur.

AIPO4 supported zinc borohydride as a novel reagent for the hydration of aromatic alkenes and alkynes

Hydration of aromatic alkenes (styrene, α-methylstyrene and E-stilbene) and alkynes (phenyl and diphenylacetylene) has been achieved by the reaction of the corresponding alkenes or alkynes or zinc borohydride combined with AIPO4 in DME. Except in the case of α-methylstyrene, Zn(BH4)2/AIPO4 provides a more efficient and selective catalytic system than the combination with SIO2 or Al2O3.