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Usage

Uses

Used in Cosmetics and Personal Care Products:
(Phenethyloxy-diphenyl-methyl)benzene is used as a fragrance ingredient for its sweet, floral scent, enhancing the aroma of cosmetics and personal care products.
Used in Perfumery:
(Phenethyloxy-diphenyl-methyl)benzene is used as a key component in perfumes and colognes, contributing to their overall fragrance profile.
Used in Soap and Detergent Production:
(Phenethyloxy-diphenyl-methyl)benzene is used as an additive in the production of soaps and detergents, providing a pleasant scent and improving the sensory experience for consumers.
Used in Household and Industrial Products:
(Phenethyloxy-diphenyl-methyl)benzene is also utilized in the formulation of various household and industrial products, where its fragrance-enhancing properties are beneficial.
Safety Note:
It is important to handle (phenethyloxy-diphenyl-methyl)benzene with care, as it can cause irritation to the skin, eyes, and respiratory system if not used properly. Appropriate safety measures should be taken during its use and handling to minimize potential adverse effects.

Upstream product

• 76-83-5 trityl chloride 
• 22096-25-9 sodium phenethylate 
• 5333-62-0 benzyl trityl ether 
• 76-84-6 triphenylmethyl alcohol 
• 60-12-8 2-phenylethanol 

Downstream Products

• 103-45-7 acetic acid phenethyl ester 
• 60-12-8 2-phenylethanol 
• 519-73-3 triphenylmethane 
• 122-78-1 phenylacetaldehyde 

Relevant academic research and scientific papers

Direct and efficient synthesis of unsymmetrical ethers from alcohols catalyzed by Fe(HSO4)3 under solvent-free conditions

Highly efficient Fe(HSO4)3 catalyzed etherification of primary, secondary and tertiary benzylic alcohols with primary and secondary aliphatic alcohols is reported. The reaction affords unsymmetrical benzyl ethers in good to excellent yields under solvent-free conditions.

A gold catalytic the method for synthesizing calls the ether

The invention provides a synthetic method of asymmetrical ether in the field of organic synthesis. The general equation of reaction is defined in the specification. In the equation, R-OH is benzyl alcohol, p-methoxy benzyl alcohol, tert-butyl alcohol, diphenyl carbinol or triphenylmethanol; and R'OH is common alkyl alcohol or a compound containing hydroxyl groups. A gold catalyst required by the reaction is Ph3PAuCl, Ph3PAuNTf2, HAuCl4, NaAuCl4, Ph3PAuOTf, Ph3PAuSbF6, IPrAuCl or nano-gold. A medium required by the reaction is solvent-free, and is toluene, mesitylene, 1,2-dichloroethane, tetrahydrofuran, acetonitrile or acetone. The reaction is implemented by heating through a microwave reactor. The method has advantages as follows: raw materials are easily available; operation is simple; the range of application is wide; atom economy is good; and the reaction is green.

Gold(I)-catalyzed synthesis of unsymmetrical ethers using alcohols as alkylating reagents

A microwave-irradiated alcohol-protecting strategy based on gold catalysis utilizing benzyl alcohol, tert-butyl alcohol and triphenylmethanol as alkylating reagents has been developed. This protecting strategy has wide functional group tolerance with satisfactory yields for the majority of the selected alcohols. The mechanism of this transformation was probed with oxygen-18 isotope labelled alcohols assisted by GC-MS techniques and chemical kinetic experiments. This strategy provides an efficient, straightforward and alternative approach to the preparation of benzyl, tert-butyl and trityl ethers in organic synthesis.

Highly efficient protection of alcohols as trityl ethers under solvent-free conditions, and recovery catalyzed by reusable nanoporous MCM-41-SO3H

An efficient method was developed for the protection of alcohols as trityl ethers using triphenylmethanol in the presence of nanoporous MCM-41-SO3H as a heterogeneous catalyst under solvent-free ball-milling at room temperature. Low catalyst loading, high efficiency, reusability are among the advantages of this new solvent-free and environmentally friendly method. The deprotection of the produced trityl ethers was also efficiently achieved using the same catalyst in wet acetonitrile.