89760-42-9

Basic information

• Product Name: 2-Propenoic acid, 3-(2-fluorophenyl)-, ethyl ester, (E)-
• Synonyms: 2-Propenoic acid, 3-(2-fluorophenyl)-, ethyl ester, (E)-
• CAS NO: 89760-42-9
• Molecular Formula: C11H11FO2
• Molecular Weight: 194.206
• Mol File: 89760-42-9.mol
• Article Data: 24

Chemical Properties

• Boiling Point: 269.0±15.0 °C(Predicted)
• Density: 1.134±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 2-Propenoic acid, 3-(2-fluorophenyl)-, ethyl ester, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenoic acid, 3-(2-fluorophenyl)-, ethyl ester, (E)-(89760-42-9)
• EPA Substance Registry System: 2-Propenoic acid, 3-(2-fluorophenyl)-, ethyl ester, (E)-(89760-42-9)

Safety Data

• Hazardous Substances Data: 89760-42-9(Hazardous Substances Data)

Usage

Structure

It is an ethyl ester derivative of 3-(2-fluorophenyl) acrylate, featuring an ethyl ester group and a fluorophenyl group attached to a 2-propenoic acid backbone.

Applications

Organic Synthesis: Used as a building block for synthesizing more complex molecules.
Pharmaceutical Research: Employed in pharmaceutical research due to its structural characteristics.
Polymer Production: Potential application in polymer production and other material synthesis.

Reactivity

Ester Group: Reactivity associated with the ester functional group.
Unsaturated Carboxylic Acid: Potential reactivity and functional properties associated with unsaturation.

Industrial Applications

Chemical Processes: Suitable for various chemical processes.
Materials Synthesis: Potential use in the synthesis of industrial materials.

Upstream product

• 462-06-6 fluorobenzene 
• 140-88-5 ethyl acrylate 
• 58686-74-1 ethyl 3-(2-fluorophenyl)propiolate 
• 867-13-0 diethoxyphosphoryl-acetic acid ethyl ester 
• 446-52-6 2-Fluorobenzaldehyde 
• 1099-45-2 ethyl (triphenylphosphoranylidene)acetate 
• 925-60-0 n-propyl acrylate 
• 348-52-7 1-Fluoro-2-iodobenzene 
• 1072-85-1 o-fluorobromobenzene 
• 64-17-5 ethanol 
• 18944-77-9 2-fluorocinnamic acid 
• 394-46-7 2-fluorostyrene 
• 1530-45-6 (carbethoxymethyl)triphenylphosphonium bromide 

Downstream Products

• 449811-16-9 6-(2-fluorobenzyl)-8-methyl-2-methylsulfanyl-8H-pyrido[2,3-d]pyrimidin-7-one 
• 449808-56-4 6-(2-fluorobenzyl)-8-methyl-2-methylsulfonyl-8H-pyrido[2,3-d]pyrimidin-7-one 
• 790652-90-3 6-(2-fluorobenzyl)-8-methyl-2-(tetrahydro-2H-pyran-4-ylamino)pyrido[2,3-d]pyrimidin-7(8H)-one 
• 39856-89-8 ethyl 3-(2-fluorophenyl)propionate 

Relevant articles and documents

Photoinduced Regioselective Olefination of Arenes at Proximal and Distal Sites

The Fujiwara-Moritani reaction has had a profound contribution in the emergence of contemporary C-H activation protocols. Despite the applicability of the traditional approach in different fields, the associated reactivity and regioselectivity issues had

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Azomethine ylides are fascinating 1,3-dipoles for [3 + 2] cycloaddition reactions toward the construction ofN-heterocycles. Herein, an efficient and environmentally benign electrochemical approach for the generation of a nonstabilized azomethine ylide has been established under metal-free and external oxidant-free conditions. The resulting 1,3-dipole undergoes a [3 + 2] cycloaddition reaction with olefins. This electrosynthetic methodology indulges a straightforward and facile approach for the construction of substituted pyrrolidines.

Selective Synthesis of Z-Cinnamyl Ethers and Cinnamyl Alcohols through Visible Light-Promoted Photocatalytic E to Z Isomerization

A photocatalytic E to Z isomerization of alkenes using an iridium photosensitizer under mild reaction conditions is disclosed. This method provides scalable and efficient access to Z-cinnamyl ether and allylic alcohol derivatives in high yields with excellent stereoselectivity. Importantly, this method also provides a powerful strategy for the selective synthesis of Z-magnolol and honokiol derivatives possessing potential biological activity.