96840-56-1

Usage

Uses

Used in Chemical Industry:
Phenol, 2-ethoxy-4-[(1-methylethoxy)methyl]is used as a chemical intermediate for the synthesis of other organic compounds. Its unique structure allows it to be a key component in the production of various chemical products.
Used in Manufacturing Resins:
Phenol, 2-ethoxy-4-[(1-methylethoxy)methyl]is used as a component in the production of resins. Its properties may contribute to the formation of resins with specific characteristics, making it a valuable ingredient in this application.
Used in Adhesives Production:
Phenol, 2-ethoxy-4-[(1-methylethoxy)methyl]is used as a component in the formulation of adhesives. Its presence may enhance the adhesive properties, providing better bonding and durability in various applications.
Used in Lubricants Industry:
Phenol, 2-ethoxy-4-[(1-methylethoxy)methyl]is used as a component in the production of lubricants. It may contribute to the lubricating properties, improving the performance and lifespan of lubricants in different industrial applications.
Used as a Solvent:
Phenol, 2-ethoxy-4-[(1-methylethoxy)methyl]may be used as a solvent in various chemical processes. Its solubility properties could make it a suitable choice for dissolving other compounds in industrial applications.
Used as a Stabilizer:
Phenol, 2-ethoxy-4-[(1-methylethoxy)methyl]may be used as a stabilizer in certain chemical formulations. Its ability to stabilize compounds could be beneficial in maintaining the consistency and performance of various products.

Upstream product

• 121-32-4 4-hydroxy-3-ethoxybenzaldehyde 
• 67-63-0 isopropyl alcohol 
• 4912-58-7 3-ethoxy-4-hydroxy-benzyl alcohol 

Relevant academic research and scientific papers

Auto-Tandem Catalysis with Frustrated Lewis Pairs for Reductive Etherification of Aldehydes and Ketones

Herein we report that a single frustrated Lewis pair (FLP) catalyst can promote the reductive etherification of aldehydes and ketones. The reaction does not require an exogenous acid catalyst, but the combined action of FLP on H2, R-OH or H2O generates the required Br?nsted acid in a reversible, “turn on” manner. The method is not only a complementary metal-free reductive etherification, but also a niche procedure for ethers that would be either synthetically inconvenient or even intractable to access by alternative synthetic protocols.

Technology for preparing vanillyl alcohol ether by using one step method

The invention relates to a technology for preparing vanillyl alcohol ether by using a one step method. The technology combines co-catalysis of a nano ruthenium metal catalyst and an immobilized tin phosphotungstate catalyst, and vanillin is subjected to a reaction for 18-24 hours under hydrogen pressure of 1-2 MPa and an alcohols solvent in a reaction vessel at the temperature of 20-60 DEG C to obtain vanillyl alcohol ether by using the one step method. The technology can be carried out under mild condition, has the advantages of environmental protection and high product yield, and is suitable for industrial production.

A general method for the preparation of ethers using water-resistant solid lewis acids

(Chemical Equation Presented) This most ethereal of cascades: Water-resistant single isolated Lewis acids within the framework of molecular sieves act as excellent general catalysts for the synthesis of ethers (see scheme). On this basis, an environmentally friendly process has been developed for the preparation of fine chemicals that involves a one-pot Meerwein-Ponndorf-Verley reduction/etherification cascade.