5467-22-1

Basic information

• Product Name: ethyl triphenylacetate
• CAS NO: 5467-22-1
• Molecular Formula: C₂₂H₂₀O₂
• Molecular Weight: 316.393
• Mol File: 5467-22-1.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 429.9°C at 760 mmHg
• Flash Point: 145.9°C
• Density: 1.107g/cm³
• Vapor Pressure: 1.36E-07mmHg at 25°C
• Refractive Index: 1.58
• CAS DataBase Reference: ethyl triphenylacetate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl triphenylacetate(5467-22-1)
• EPA Substance Registry System: ethyl triphenylacetate(5467-22-1)

Safety Data

• Hazardous Substances Data: 5467-22-1(Hazardous Substances Data)

Usage

General Description

Ethyl triphenylacetate is a chemical compound with the molecular formula C22H20O2. It is a colorless, fragrant liquid that is commonly used in the fragrance and flavor industry. Ethyl triphenylacetate has a sweet, floral scent and is often used as a fixative in perfumes and as a flavoring agent in food products and beverages. It is also used in the production of pharmaceuticals and as a chemical intermediate in organic synthesis. Ethyl triphenylacetate is considered to be relatively stable and has low toxicity, making it a versatile and safe ingredient in various consumer products.

Upstream product

• 917-64-6 methyl magnesium iodide 
• 60-29-7 diethyl ether 
• 6068-70-8 triphenylacetyl chloride 
• 4303-71-3 triphenylmethyl sodium 
• 541-41-3 chloroformic acid ethyl ester 
• 74-96-4 ethyl bromide 
• 595-91-5 triphenylacetic acid 
• 101-97-3 Ethyl 2-phenylethanoate 
• 1483-72-3 diphenyliodonium chloride 
• 76-83-5 trityl chloride 
• 78-39-7 Triethyl orthoacetate 
• 75-03-6 ethyl iodide 
• 3468-99-3 ethyl diphenylacetate 
• 105-58-8 Diethyl carbonate 

Downstream Products

• 519-73-3 triphenylmethane 
• 15719-64-9 methylammonium carbonate 
• 1016970-45-8 1,1-dideuterio-2,2,2-triphenylethanol 
• 595-91-5 triphenylacetic acid 

Relevant articles and documents

Gold(I)-catalyzed double migration cascades toward (1E,3E)-dienes and naphthalenes

A novel gold(I)-catalyzed cascade cycloisomerization of a variety of propargylic esters leading to unsymmetrically substituted naphthalenes has been developed. This domino process involves an unprecedented tandem sequence of 1,3- and 1,2-migrations of two

Efficient esterification of carboxylic acids and phosphonic acids with trialkyl orthoacetate in ionic liquid

An operationally simple, inexpensive, efficient, and environmentally friendly esterification of various carboxylic acids, phosphonic acids, and phosphinic acids with triethyl orthoacetate or trimethyl orthoacetate under neutral conditions in a typical room temperature ionic liquid, 1-butyl-3-methylimidazolium hexafluorophosphate, was successfully carried out to provide the corresponding ethyl esters or methyl esters in high yields.

CsF-Promoted Esterification of Carboxylic Acids. A Practical Alternative to the Diazomethane Method and Direct Conversion of Organotin Carboxylates

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