100764-07-6

Usage

Uses

Used in Flavor and Fragrance Industry:
(E)-2-ethyl-4-phenylbut-2-enal is used as a flavoring agent for its fruity, floral, and sweet odor, enhancing the taste and aroma of various food and beverages.
(E)-2-ethyl-4-phenylbut-2-enal is used as a fragrance ingredient in the production of perfumes and scented consumer products, such as soaps, lotions, and air fresheners, due to its pleasant and appealing floral scent.
Used in Pharmaceutical Industry:
(E)-2-ethyl-4-phenylbut-2-enal is used as a precursor in the synthesis of pharmaceuticals, contributing to the development of new drugs and medications.
Used in Organic Chemical Reactions:
(E)-2-ethyl-4-phenylbut-2-enal serves as a starting material or intermediate in various organic chemical reactions, facilitating the creation of a wide range of chemical products and compounds.

Upstream product

• 30989-69-6 2-(diethoxymethyl)-1,1-diethoxybutane 
• 201230-82-2 carbon monoxide 
• 370867-96-2 (+/-)-(E)-2-[2-(diphenylphosphanyl)benzoyloxy]-1-phenyl-3-pentene 
• 100764-29-2 Potassium; (Z)-2-formyl-but-1-en-1-olate 
• 100-44-7 benzyl chloride 
• 100764-03-2 2-[1-Trimethylsilanyloxy-meth-(E)-ylidene]-butyraldehyde 

Relevant academic research and scientific papers

Directed regio- and stereoselective hydroformylation of mono- and 1,3-disubstituted allylic alcohols: A catalytic approach to the anti-aldol-retron

Regioselective and diastereoselective hydroformylation of mono- and 1,3-disubstituted allylic alcohol o-DPPB esters is described. The products represent synthetically important anti-aldol retrons.

Tandem-directed regioselective hydroformylation/β-elimination: A practical method for the synthesis of enals

A practical synthesis of α,β-unsaturated aldehydes by a tandem-directed hydroformylation/β-elimination process of allylic o-DPPB esters is reported. The o-DPPB group served as an effective controller for regioselectivity of the hydroformylation towards th

Oxopropenylation of Alkylmagnesium Halides by 3-(Trimethylsilyloxy)acroleins

Oxopropenylation of alkylmagnesium halides 4 by 3-(trimethylsilyloxy)acroleins 3 selectively yields the (E)-isomers of α,β-unsaturated aldehydes such as 4-phenyl-2-butenals 9, 3-cyclopropylpropenals 10, 3-cyclohexylpropenals 11, 3-(3-menthyl)propenals 12, and 2,5-hexadienals 13. 3-Hydroxyenolsilylethers 6 are isolated when allylmagnesium chloride is used as carbon nucleophile; to conclude, the reaction primarily involves nucleophilic addition of the Grignard reagent at the aldehyde carbon of the acrolein 3.