38495-73-7

Basic information

• Product Name: 1-(4-ethoxyphenyl)-2-phenylethanone
• Synonyms: ethanone, 1-(4-ethoxyphenyl)-2-phenyl-
• CAS NO: 38495-73-7
• Molecular Formula: C₁₆H₁₆O₂
• Molecular Weight: 240.297
• Mol File: 38495-73-7.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 392.4°C at 760 mmHg
• Flash Point: 175.3°C
• Density: 1.081g/cm³
• Vapor Pressure: 2.3E-06mmHg at 25°C
• Refractive Index: 1.562
• CAS DataBase Reference: 1-(4-ethoxyphenyl)-2-phenylethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-ethoxyphenyl)-2-phenylethanone(38495-73-7)
• EPA Substance Registry System: 1-(4-ethoxyphenyl)-2-phenylethanone(38495-73-7)

Safety Data

• Hazardous Substances Data: 38495-73-7(Hazardous Substances Data)

Usage

Description

1-(4-ethoxyphenyl)-2-phenylethanone, also known as ethyl 4-ethoxyphenyl phenylacetate, is a chemical compound with the molecular formula C17H18O2. It is a pale yellow, oily liquid characterized by a floral and fruity odor. 1-(4-ethoxyphenyl)-2-phenylethanone is valued for its diverse applications across various industries, including its use in the production of fragrances and flavors, as an intermediate in the synthesis of pharmaceuticals and organic compounds, and for its potential antimicrobial, antioxidant, and antiviral properties in healthcare products.

Uses

Used in Fragrance and Flavor Industry:
1-(4-ethoxyphenyl)-2-phenylethanone is used as a key ingredient for creating fragrances and flavors due to its pleasant and appealing scent. Its distinctive floral and fruity odor makes it a popular choice for enhancing the aroma of various products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1-(4-ethoxyphenyl)-2-phenylethanone is utilized as an intermediate in the synthesis of various drugs and organic compounds. Its chemical properties allow it to serve as a building block for developing new medications.
Used in Healthcare Products:
1-(4-ethoxyphenyl)-2-phenylethanone is used as an additive in the development of healthcare products due to its potential antimicrobial, antioxidant, and antiviral properties. These characteristics make it a valuable component in products aimed at promoting health and well-being.
Overall, 1-(4-ethoxyphenyl)-2-phenylethanone demonstrates a broad spectrum of applications, making it a versatile and essential compound in the fragrance, flavor, pharmaceutical, and healthcare industries.

Upstream product

• 74-96-4 ethyl bromide 
• 2491-32-9 1-(4-Hydroxyphenyl)-2-phenylethanone 
• 860598-03-4 1-(4-ethoxy-phenyl)-2-amino-1-phenyl-ethanol 
• 103-73-1 Phenetole 
• 103-80-0 phenylacetyl chloride 
• 64-19-7 acetic acid 
• 5459-40-5 4-ethoxystyrene 
• 100-63-0 phenylhydrazine 

Downstream Products

• 39229-13-5 4-ethoxybenzil 
• 20458-79-1 4-ethoxy-α-bromo-deoxybenzoin 
• 28181-63-7 4-ethoxy-bibenzyl-α-ol 
• 87299-03-4 5-Benzyl-5-(4-ethoxy-phenyl)-imidazolidine-2,4-dione 
• 86029-57-4 (+/-)-5-(4-ethoxy-phenyl)-5-phenyl-imidazolidine-2,4-dione 
• 87299-10-3 3a-(4-Ethoxy-phenyl)-6a-phenyl-tetrahydro-imidazo[4,5-d]imidazole-2,5-dione 
• 124115-16-8 3-(4-ethoxy-phenyl)-2,4,5-triphenyl-cyclopentadienone 
• 1243643-44-8 2-(4-ethoxyphenyl)-1-phenyl-4-p-tolylbut-3-yn-2-ol 

Relevant articles and documents

Catalyst-controlled highly selective coupling and oxygenation of olefins: A direct approach to alcohols, ketones, and diketones

Oxygen? That's radical! A method for the direct synthesis of substituted alcohols, ketones, and diketones through a catalyst-controlled highly chemoselective coupling and oxygenation of olefins has been developed. The method is simple and practical, can be switched by the selection of different catalysts, and employs molecular oxygen as both an oxidant and a reagent. Copyright