31516-55-9

Basic information

• Product Name: 2,4-Diphenyl-2-methylpentane
• Synonyms: 2,4-Diphenyl-2-methylpentane;2,4-Diphenyl-4-methylpentane;2-Methyl-2,4-diphenylpentane;4-Methyl-2,4-diphenylpentane
• CAS NO: 31516-55-9
• Molecular Formula: C₁₈H₂₂
• Molecular Weight: 238.37
• Mol File: 31516-55-9.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,4-Diphenyl-2-methylpentane(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-Diphenyl-2-methylpentane(31516-55-9)
• EPA Substance Registry System: 2,4-Diphenyl-2-methylpentane(31516-55-9)

Safety Data

• Hazardous Substances Data: 31516-55-9(Hazardous Substances Data)

Usage

General Description

2,4-Diphenyl-2-methylpentane is a chemical compound with the molecular formula C19H24. It is a colorless, odorless liquid at room temperature and is insoluble in water but soluble in organic solvents. It is commonly used as a building block in the synthesis of various organic compounds. This chemical has a high purity and is stable under normal conditions, making it suitable for use in pharmaceutical and industrial applications. It is also a versatile compound with potential applications in research and development of new materials and products. However, it is important to handle 2,4-Diphenyl-2-methylpentane with care and follow proper safety precautions due to its potential hazards.

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 articles and documents

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.

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.

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.