718-25-2

Basic information

• Product Name: 1-FLUORO-4-((E)-STYRYL)-BENZENE
• Synonyms: 1-FLUORO-4-((E)-STYRYL)-BENZENE;(E)-4-Fluorostilbene
• CAS NO: 718-25-2
• Molecular Formula: C₁₄H₁₁F
• Molecular Weight: 198.2355432
• Mol File: 718-25-2.mol
• Article Data: 198

Chemical Properties

• Boiling Point: 287.3°C at 760 mmHg
• Flash Point: 124.2°C
• Appearance: /
• Density: 1.12g/cm³
• Vapor Pressure: 0.00433mmHg at 25°C
• Refractive Index: 1.639
• CAS DataBase Reference: 1-FLUORO-4-((E)-STYRYL)-BENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-FLUORO-4-((E)-STYRYL)-BENZENE(718-25-2)
• EPA Substance Registry System: 1-FLUORO-4-((E)-STYRYL)-BENZENE(718-25-2)

Safety Data

• Hazardous Substances Data: 718-25-2(Hazardous Substances Data)

Usage

Structure

Benzene derivative with a fluorine atom at the 1-position and a styryl group at the 4-position

Type of Compound

Organic compound

Fluorescence Properties

Exhibits fluorescence, useful in materials science and as a fluorescent probe in biological studies

Applications

Building block in organic synthesis, potential use in pharmaceuticals, agrochemicals, and fine chemicals production

Research and Development

Interesting target for research and development in various fields due to its unique structure and properties

InChI:InChI=1/C14H11F/c15-14-10-8-13(9-11-14)7-6-12-4-2-1-3-5-12/h1-11H/b7-6+

Upstream product

• 352-34-1 4-fluoro-1-iodobenzene 
• 155857-33-3 1--1-phenylethene 
• 122-78-1 phenylacetaldehyde 
• 460-00-4 1-Bromo-4-fluorobenzene 
• 100-52-7 benzaldehyde 
• 459-46-1 4-Fluorobenzyl bromide 
• 405-50-5 p-Fluorophenylacetic acid 
• 618-31-5 benzylidene dibromide 
• 349483-17-6 N-(4-fluorobenzylidene)-propan-1-amine 
• 1100-88-5 benzyltriphenylphosphonium chloride 
• 459-57-4 4-fluorobenzaldehyde 
• 100-42-5 styrene 
• 405-29-8 (4-fluorophenyl)phenylacetylene 
• 405-99-2 para-fluorostyrene 

Downstream Products

• 1436919-11-7 (E)-1-methyl-4-(4-styrylphenoxy)benzene 
• 1448661-17-3 trans-1-(3-phenylpropoxy)-4-styrylbenzene 
• 1448661-26-4 trans-1-ethoxy-4-(4-styrylphenoxy)benzene 
• 1448661-27-5 trans-1-propyl-4-(4-styrylphenoxy)benzene 
• 1448661-28-6 trans-2-(4-styrylphenoxy)naphthalene 
• 24265-92-7 (E)-1-(4-benzyloxyphenyl)-2-phenylethene 
• 1657-46-1 cis-4-fluorostilbene 
• 52881-64-8 2-(4-fluorophenyl)-3-phenyloxirane 
• 345-83-5 4-fluorobenzophenone 
• 3834-66-0 (4-fluorophenyl)phenylethanedione 

Relevant articles and documents

Suzuki coupling reactions in neat water as the solvent: Where in the biphasic reaction mixture do the catalytic reaction steps occur?

Many reports on water-compatible palladium catalysts have appeared in the recent literature. For hydrophobic substrates, mixtures with pure water are biphasic, and it is widely not regarded that the elusive locality of the catalytic process (in water, the

Pd-Catalyzed Coupling of N-Tosylhydrazones with Benzylic Phosphates: Toward the Synthesis of Di- or Tri-Substituted Alkenes

This study shows that various di- and tri-substituted alkenes with high chemoselectivity were obtained in good to high yields by coupling N-tosylhydrazones (NTHs) with benzylic phosphates as electrophilic partners. The obtained new catalytic system consis

Pd-Catalyzed Cross-Coupling of Organostibines with Styrenes to Give Unsymmetric (E)-Stilbenes and (1 E,3 E)-1,4-Diarylbuta-1,3-dienes and Fluorescence Properties of the Products

A general and effective palladium-catalyzed cross-coupling of organostibines with styrenes to give (E)-olefins was disclosed. By the use of an organostibine reagent, this method can produce unsymmetric (E)-1,2-diarylethylenes and (1E,3E)-1,4-diarylbuta-1,3-dienes in good yields with high E/Z selectivity and good functional group tolerance. Resveratrol and DMU-212 were synthesized in high yield. The protocol can be extended to the synthesis of (1E,3E,5E)-1,6-diphenylhexa-1,3,5-triene in 40% yield. Products 5e, 5f, and 7a showed good photoluminescence quantum yields ranging from 72 to 99%.