93805-71-1

Usage

Uses

Used in Solvent Applications:
[2,2-bis(1-methylethoxy)ethyl]benzene is used as a solvent in various industrial processes due to its high solvent power and low volatility. It is particularly effective in dissolving a wide range of substances, making it a versatile choice for numerous applications.
Used in Chemical Intermediate Applications:
[2,2-bis(1-methylethoxy)ethyl]benzene serves as a chemical intermediate in the synthesis of other chemicals and products. Its unique properties allow it to be a valuable component in the creation of various compounds used across different industries.
Used in Polymer and Resin Production:
[2,2-bis(1-methylethoxy)ethyl]benzene is used as an additive in the production of polymers and resins, where its properties contribute to enhancing the final product's performance characteristics.
Used in Coatings and Adhesives Industry:
[2,2-bis(1-methylethoxy)ethyl]benzene is utilized in the coatings and adhesives industry, benefiting from its high solvent power and low volatility. These properties make it suitable for use in high-performance applications, such as creating durable and long-lasting coatings and adhesives.
Safety Precautions:
While [2,2-bis(1-methylethoxy)ethyl]benzene offers numerous industrial applications, it is essential to note that it may pose health hazards if inhaled, ingested, or comes into contact with the skin. Therefore, proper safety precautions should be followed when handling [2,2-bis(1-methylethoxy)ethyl]benzene to ensure the well-being of individuals working with it.

InChI:InChI=1/C14H22O2/c1-11(2)15-14(16-12(3)4)10-13-8-6-5-7-9-13/h5-9,11-12,14H,10H2,1-4H3

Upstream product

• 100-42-5 styrene 
• 67-63-0 isopropyl alcohol 
• 1118-30-5 propanone diisopropyl acetal 
• 101-48-4 phenylacetaldehyde dimethyl acetal 

Downstream Products

• 2154-56-5 benzyl radical 
• 44844-54-4 C₇H₁₅O₂⁽¹⁺⁾ 
• 14371-21-2 [2-(1-methylethoxy)-ethenyl]-benzene 
• 70064-30-1 [2-(1-methylethoxy)-ethenyl]-benzene 

Relevant academic research and scientific papers

Effective Au(III)-CuCl2-catalyzed addition of alcohols to alkenes

Alkenes can be activated by Au(III) catalysts, and the effective addition of alcohols to alkenes can be carried out under mild conditions with Au(III), provided that catalytic amounts of CuCl2 are added, which significantly stabilize the cationic Au(III). The Royal Society of Chemistry.

The Mechanism of Termal Eliminations. Part 26. Substituent Effects at Each Carbon of Vinyl Ethers: Non-planarity of the Transition State

A range of 1-arylethyl vinyl ethers and 1-arylvinyl isopropyl ethers, 2-phenylethyl vinyl ether, isopropenyl isopropyl ether, and isopropyl cis- and trans-phenylvinyl ether have been synthesized and their rates of termal elimination measured between 585.9-666.4 K.The Ei mechanism for vinyl ether pyrolysis has less E1 character than that for pyrolysis of the corresponding esters, so nucleophilic attack by the double bond upon the β-hydrogen is more important for the former.Electron supply to the double bond therefore increases the pyrolysis rate, so that isopropenyl isopropyl ether is more reactive than isopropyl vinyl ether (5.85-fold at 600 K), whereas acetates and formates are almost equally reactive.Likewise isopropyl 1-phenylvinyl ether is 2.2 times more reactive than isopropenyl isopropyl ether,slightly greater than the reactivity difference between the corresponding esters (benzoates and acetates).The rate-enhancing effect of a 2--phenyl substituent in ethyl vinyl ether (5.81-fold per β-hydrogen) is a little less than the corresponding effect in ethyl acetate.In the 2-phenylvinyl ethers both cis and trans phenyl groups produce slight rate acceleration, due to the combined effects of loss of conjugation on going to products, and increase in electron supply to the double bond.The trans compound is more reactive than the cis, confirming that the six-membered transition state for β-elimination is not planar.Aryl substituents in 1-arylvinyl isopropyl ethers produce only very small rate effects; the effects could not be determined for electron-supplying substituents because these induced very rapid oxidation to isopropyl benzoates, and atmospheric hydrolysis also occurs.Isopropyl 2-phenylvinyl ethers were likewise oxidized to benzaldehyde and isopropyl formate. 1-Arylethyl vinyl ethers eliminate abnormally rapidly with concurrent rearrangements to aldehydes and other products.