70592-05-1

Basic information

• Product Name: 1-methoxy-4-(1,2,2-triphenylethenyl)Benzene
• Synonyms: 1-methoxy-4-(1,2,2-triphenylethenyl)Benzene
• CAS NO: 70592-05-1
• Molecular Formula: C₂₇H₂₂O
• Molecular Weight: 362.46298
• EINECS: -0
• Mol File: 70592-05-1.mol
• Article Data: 23

Chemical Properties

• Melting Point: 131-132 °C
• Boiling Point: 461.0±14.0 °C(Predicted)
• Appearance: /
• Density: 1.099±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 1-methoxy-4-(1,2,2-triphenylethenyl)Benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-methoxy-4-(1,2,2-triphenylethenyl)Benzene(70592-05-1)
• EPA Substance Registry System: 1-methoxy-4-(1,2,2-triphenylethenyl)Benzene(70592-05-1)

Safety Data

• Hazardous Substances Data: 70592-05-1(Hazardous Substances Data)

Usage

Structure

Consists of a benzene ring substituted with a methoxy group and a triphenylethylene group

Appearance

Colorless solid

Solubility

Insoluble in water, soluble in organic solvents

Uses

Commonly used as a starting material in the synthesis of various organic compounds and as a fluorescent dye in biological and chemical research

Optical properties

Exhibits strong fluorescence when exposed to ultraviolet light, making it useful in the field of optics and photonics

Therapeutic applications

Potential ability to inhibit the growth of cancer cells and its antioxidant properties

Upstream product

• 1607-57-4 Triphenylvinyl bromide 
• 100-66-3 methoxybenzene 
• 25354-48-7 1-bromo-1-(p-methoxyphenyl)-2,2-diphenylethene 
• 71-43-2 benzene 
• 780756-27-6 4-tert-butyl-2-[1-(4-methoxy-phenyl)-2,2-diphenyl-vinylsulfanyl]-pyrimidine 
• 76115-05-4 1-(4'-methoxyphenyl)-1,2,2-triphenylethanol 
• 611-94-9 4-Methoxybenzophenone 
• 119-61-9 benzophenone 
• 1484-50-0 desyl bromide 
• 2524-64-3 chlorophosphoric acid diphenyl ester 
• 101-81-5 Diphenylmethane 
• 591-50-4 iodobenzene 
• 501-65-5 diphenyl acetylene 
• 13139-86-1 4-methoxyphenyl magnesium bromide 

Downstream Products

• 76115-06-5 1-(4'-hydroxyphenyl)-1,2,2-triphenylethylene 
• 1471339-65-7 2-[4-(1,2,2-triphenylethenyl)phenoxy]acetic acid 

Relevant articles and documents

Room-Temperature Negishi Reaction of Trisubstituted Vinyl Phosphates for the Synthesis of Tetrasubstituted Alkenes

The present study investigated the ability of bromovinyl phosphates to react with organozinc reagents at room temperature during palladium-catalyzed reactions. It was determined that both the bromine atom and the phosphate group were successfully substituted by means of the reaction with the organozinc reagents, thereby allowing for the synthesis of cyclic and acyclic tetrasubstituted double bonds. The low stability of the organozinc compounds in an acidic environment was exploited to accomplish the synthesis of alkenes using a one-pot, two-step experimental setup.

Aggregation-induced emission molecular compound, preparation method and application thereof

The invention discloses an aggregation-induced emission molecular compound. The aggregation-induced emission molecular compound comprises a monosubstituted tetraphenyl ethylene derivative taking tetraphenyl ethylene as a skeleton, or a heavy atom-containi

Synthesis of Tetraarylethene Luminogens by C?H Vinylation of Aromatic Compounds with Triazenes

Tetraarylethenes are obtained by acid-induced coupling of vinyl triazenes with aromatic compounds. This new C?H activation route for the synthesis of aggregation-induced emission luminogens is simple, fast, and versatile. It allows the direct grafting of triarylethenyl groups onto a variety of aromatic compounds, including heterocycles, supramolecular hosts, biologically relevant molecules, and commercial polymers.