5467-22-1

Usage

Uses

Used in Fragrance Industry:
Ethyl triphenylacetate is used as a fixative in perfumes for its ability to enhance and prolong the scent of other fragrance components.
Used in Flavor Industry:
In the flavor industry, ethyl triphenylacetate is used as a flavoring agent in food products and beverages, imparting a sweet, floral taste.
Used in Pharmaceutical Production:
Ethyl triphenylacetate is utilized in the production of pharmaceuticals, contributing to the development of various medicinal formulations.
Used as a Chemical Intermediate in Organic Synthesis:
In the field of organic synthesis, ethyl triphenylacetate serves as a chemical intermediate, facilitating the synthesis of other complex organic compounds.

Upstream product

• 60-29-7 diethyl ether 
• 4303-71-3 triphenylmethyl sodium 
• 541-41-3 chloroformic acid ethyl ester 
• 30615-54-4 triphenylmethyl bromide 
• 105-58-8 Diethyl carbonate 
• 101-97-3 Ethyl 2-phenylethanoate 
• 74-96-4 ethyl bromide 
• 595-91-5 triphenylacetic acid 
• 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 
• 64-17-5 ethanol 

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 academic research and scientific papers

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

Gold-catalyzed double migration-benzannulation cascade toward naphthalenes

(Chemical Equation Presented) A novel gold(I)-catalyzed cycloisomerization of propargylic esters leading to unsymmetrically substituted naphthalenes has been developed. This cascade reaction involves an unprecedented tandem sequence of 1,3- and 1,2-migration of two different migrating groups. It is believed that this transformation likely proceeds via the formation of 1,3-diene intermediate or its precursor, which upon cyclization and aromatization steps transforms into the naphthalene core. 2008 American Chemical Society.

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.

Environmentally friendly esterification of carboxylic acids with triethyl orthoacetate in ionic liquid

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