17655-74-2

Usage

Uses

Used in the Chemical Industry:
[(E)-2-ethoxyethenyl]benzene is used as a solvent for various applications due to its ability to dissolve a wide range of substances. Its solvent properties make it a valuable asset in the chemical industry for processes that require the use of a reliable and effective solvent.
Used in the Fragrance Industry:
In the realm of fragrances, [(E)-2-ethoxyethenyl]benzene is utilized as a key component. Its sweet, floral odor contributes to the creation of various scents, making it a sought-after ingredient in the formulation of perfumes and other aromatic products.
Used in the Synthesis of Other Chemicals:
[(E)-2-ethoxyethenyl]benzene also serves as an intermediate in the synthesis of other chemicals. Its unique chemical structure allows it to be a versatile building block in the production of a variety of compounds, further expanding its utility and importance in the chemical industry.

Upstream product

• 103-64-0 bromostyrene 
• 141-52-6 sodium ethanolate 
• 29969-69-5 3,3-diethoxy-2-phenyl-propionic acid 
• 536-74-3 phenylacetylene 
• 4819-77-6 1,1,2-triethoxyethane 
• 23521-49-5 (Z)-1-bromo-2-ethoxyethene 
• 16721-45-2 triphenyl(phenylmethylene)phosphorane 
• 109-94-4 formic acid ethyl ester 
• 64-17-5 ethanol 
• 622-25-3 1-(2-chlorovinyl)benzene 
• 6314-97-2 1,1-diethoxy-2-phenylethane 
• 39153-68-9 (E,Z)-β-phenoxystyrene 
• 932-88-7 1-iodo-2-phenylethyne 
• 17838-69-6 ethyl 3-oxo-2-phenylpropanoate 

Downstream Products

• 92854-55-2 2-ethoxy-5,6,7,8-tetrachloro-3-phenyl-2,3-dihydro-benzo[1,4]dioxin 
• 122-78-1 phenylacetaldehyde 
• 1152-17-6 phenyl(3-phenylisoxazol-5-yl)methanone 
• 127704-23-8 1,1,3,5,5-pentaethoxy-2-phenylpentane 
• 127704-51-2 1,1,3,5,7,7-hexaethoxy-2,6-diphenylheptane 
• 127704-54-5 1,1,3,7,7-pentaethoxy-2-phenyl-4-heptene 
• 127704-57-8 1,1,3,7,7-pentaethoxy-2,5-diphenyl-4-heptene 
• 64-17-5 ethanol 
• 71598-83-9 7,16-diphenyldibenzo<1,4,8,11>-tetraaza<14>annulene 
• 26591-66-2 2-phenyl-1,3-propanedial 
• 3920-25-0 2-phenyl-3-anilino-N-phenylprop-2-enimine 
• 1357012-32-8 N-methyl-N-(3-phenylnaphthalen-2-yl)methanesulfonamide 
• 278167-61-6 1-(p-toluenesulfonyl)-3-(p-methoxyphenyl)-4-phenyl-1H-pyrrole 

Relevant academic research and scientific papers

Palladium-catalyzed synthesis of α-aryl acetophenones from styryl ethers and aryl diazonium saltsviaregioselective Heck arylation at room temperature

Preparation of α-aryl acetophenones from styryl ethers and aryldiazonium salts is described. The reaction is catalyzed by palladium acetate at room temperature in the absence of ligand and base. The developed method is highly attractive in terms of reaction conditions, substrate scope, functional group tolerance and yields. Synthetic applications of the present method are demonstrated by preparing α-aryl indoles and 3-aryl isocoumarin from styryl ethers.

Cesium hydroxide catalyzed addition of alcohols and amine derivatives to alkynes and styrene

In the presence of catalytic amounts of cesium hydroxide (CsOH · H2O), alcohols, substituted anilines and heterocyclic amines undergo an addition in NMP to phenylacetylene leading to functionalized enol ethers and enamines. Anilines add to styrene (90-120°C, 12-14 h) leading to N-substituted anilines in satisfactory yields.

Titanium-Mediated Carbonyl Olefinations. 2. Benzylidenations of Carbonyl Compounds with Dibenzyltitanocene

Mild thermolysis of carbonyl compounds with dibenzyltitanocene affords phenyl-substituted olefins, enol ethers, and enamines.