26232-98-4

Usage

Uses

Used in Pharmaceutical Industry:
CIS-4,4-DIMETHYL-2-PENTENE is used as a chemical intermediate for the production of various pharmaceuticals. Its unique properties allow it to be a key component in the synthesis of drugs, contributing to the development of new medications and therapies.
Used in Fragrance Industry:
In the fragrance industry, CIS-4,4-DIMETHYL-2-PENTENE is utilized as a chemical intermediate to create distinct and appealing scents. Its sweet, fruity odor makes it a valuable contributor to the formulation of perfumes, colognes, and other fragrance products.
Used in Organic Chemical Production:
CIS-4,4-DIMETHYL-2-PENTENE also serves as a chemical intermediate in the production of other organic chemicals. Its versatility in chemical reactions enables it to be a part of the synthesis process for a diverse range of organic compounds, expanding its applications across various industries.
Used as an Industrial Solvent:
Furthermore, CIS-4,4-DIMETHYL-2-PENTENE is employed as a solvent in certain industrial processes. Its ability to dissolve certain substances makes it a useful component in various applications, aiding in the efficiency and effectiveness of these processes.
Safety Precautions:

Upstream product

• 118791-69-8 3-bromo-2,2-dimethyl-pentane 
• 3970-62-5 2,2-dimethyl-3-pentanol 
• 6144-93-0 4.4-Dimethyl-2-pentanol 
• 7664-93-9 sulfuric acid 
• 762-62-9 4,4-dimethylpent-1-ene 
• 592-27-8 2-methylheptane 
• 187737-37-7 propene 

Downstream Products

• 590-35-2 2,2-dimethylpentane 
• 10574-37-5 2,3-dimethylpent-2-ene 
• 35623-61-1 2,2,3r,4t-tetramethyl-1-phenyl-phosphetane 1t-oxide 
• 856339-05-4 3,4-dibromo-2,2-dimethyl-pentane 
• 32278-29-8 4-bromo-2,2-dimethylpentan-3-one 

Relevant academic research and scientific papers

Surface versus molecular siloxy ligands in well-defined olefin metathesis catalysts: [{(RO)3SiO}Mo(=NAr)(=CHtBu)(CH2tBu)]

Surface organometallic chemistry: Similar electronic properties of molecular and surface siloxy ligands in 1 m and 1 were revealed by a structural investigation with solid-state NMR spectroscopy and a reactivity study in olefin metathesis. Despite similar initial turnover frequencies, the silica-supported catalyst 1 is more stable than 1 m and allows it to achieve higher turnovers, thus showing the advantage of site isolation on surfaces. (Figure Presented)

Etudes des reactions d'oxydation du n-heptane et de l'isooctane

The oxidation mechanisms of two alkanes that have quite different octane numbers: n-heptane (0) and isooctane (100), were investigated to obtain a better understanding of the chemical mechanism of autoignition phenomena and to improve the compatibility of the available fuels with the engines.The experimental study was performed at 923 K in a setup equipped with a jet-stirred reactor.The oxidation mechanisms of n-heptane and isooctane were simplified first by a purely kinetic analysis based on the product formation and then by using a software of simulation of reaction mechanisms.The very different behaviour of these two hydrocarbons was explained by the presence, in the products of isooctane oxidation, of alkenes, which would have an antiknock effect due to the formation of resonance-stabilized radicals. - Keywords: oxidation reaction; n-heptane; isooctane; autoignition; modelling