4356-69-8

Basic information

• Product Name: 1,1-Bis(p-anisyl)ethene
• Synonyms: 1,1-Bis(p-anisyl)ethene;1,1-Bis(p-methoxyphenyl)ethene;1,1-Di(p-anisyl)ethene;1,1-Di-p-anisylethene;4,4'-(Ethene-1,1-diyl)bisanisole;4,4'-Ethenylidenebis(1-methoxybenzene);4,4'-(ethene-1,1-diyl)bis(methoxybenzene)
• CAS NO: 4356-69-8
• Molecular Formula: C₁₆H₁₆O₂
• Molecular Weight: 240.297
• Mol File: 4356-69-8.mol
• Article Data: 77

Chemical Properties

• Melting Point: 142-143 °C
• Boiling Point: 381.3°Cat760mmHg
• Flash Point: 153.5°C
• Appearance: /
• Density: 1.045g/cm³
• CAS DataBase Reference: 1,1-Bis(p-anisyl)ethene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1-Bis(p-anisyl)ethene(4356-69-8)
• EPA Substance Registry System: 1,1-Bis(p-anisyl)ethene(4356-69-8)

Safety Data

• Hazardous Substances Data: 4356-69-8(Hazardous Substances Data)

Usage

General Description

1,1-Bis(p-anisyl)ethene is a chemical compound with the molecular formula C20H22O. It is an organic compound that consists of two p-anisyl groups attached to a central ethene group. 1,1-Bis(p-anisyl)ethene is commonly used as a fluorescent probe for detecting free radicals and other reactive oxygen species. It is also used as a sensitizer in organic photovoltaic devices and as a monomer for the synthesis of polymers. 1,1-Bis(p-anisyl)ethene has the potential to be used in various fields including medicine, materials science, and electronics due to its unique properties and versatile applications. However, it is important to handle this compound with caution as it may pose health and environmental risks if not properly managed.

Upstream product

• 62897-80-7 2-bromo-1,1-bis-(4-methoxy-phenyl)-ethane 
• 93903-64-1 3,3-bis-(4-methoxy-phenyl)-butyric acid 
• 66110-26-7 3,3-bis(4-methoxyphenyl)pentanedioic acid 
• 100-66-3 methoxybenzene 
• 2196-99-8 2-chloro-1-(4-methoxyphenyl)ethanone 
• 67-56-1 methanol 
• 2132-64-1 2,2-bis-(p-methoxyphenyl)-1-bromoethylene 
• 90-96-0 bis(p-methoxyphenyl)methanone 
• 1779-49-3 Methyltriphenylphosphonium bromide 
• 75-05-8 acetonitrile 
• 2032-35-1 Bromoacetaldehyde diethyl acetal 
• 621-62-5 chloroacetaldehyde diethyl acetal 
• 60-29-7 diethyl ether 
• 10026-13-8 phosphorus pentachloride 

Downstream Products

• 18813-83-7 (+/-)-9-methoxy-8-(4-methoxy-phenyl)-(4ar)-1,2,3,4,4a,5,6,7-octahydro-1t,4t-etheno-naphthalene-2t,3t,5t,6t-tetracarboxylic acid-2,3;56-dianhydride 
• 17792-18-6 3,3-bis(4-methoxyphenyl)propenoic acid 
• 102591-99-1 3,3-bis-(4-methoxy-phenyl)-acrylic acid phenyl ester 
• 96179-43-0 3,3-bis(4-methoxyphenyl)-N-(naphthalen-1-yl)acrylamide 
• 112551-63-0 3,3-bis-(4-methoxy-phenyl)-acrylic acid-(4-nitro-anilide) 
• 54655-89-9 1,1,4,4-tetrakis(4-methoxyphenyl)butadiene 
• 63153-81-1 [2,2-bis-(4-methoxy-phenyl)-vinyl]-(4-nitro-phenyl)-diazene 
• 94905-41-6 4,4-bis-(4-methoxy-phenyl)-2-oxo-but-3-enenitrile 
• 36697-31-1 2,2-bis-(p-methoxyphenyl)-1-nitroethylene 
• 115020-16-1 1,1-bis-(4-methoxy-phenyl)-2-(2-nitro-phenylselanyl)-ethene 
• 72735-91-2 2-Methoxy-5-(4-methoxyphenyl)-benzanthracene-7,12-dione 
• 93404-12-7 2-chloro-3-<2,2-bis(p-methoxyphenyl)ethenyl>-1,4-naphthoquinone 
• 104267-18-7 7-Methoxy-1,1,4-tris-(4-methoxy-phenyl)-1,2-dihydro-naphthalene 
• 90-96-0 bis(p-methoxyphenyl)methanone 

Relevant articles and documents

Photoinduced Hydroarylation and Cyclization of Alkenes with Luminescent Platinum(II) Complexes

Photoinduced hydroarylation of alkenes is an appealing synthetic strategy for arene functionalization. Herein, we demonstrated that aryl radicals generated from electron-deficient aryl chlorides/bromides could be trapped by an array of terminal/internal aryl alkenes in the presence of [Pt(O^N^C^N)] under visible-light (410 nm) irradiation, affording anti-Markovnikov hydroarylated compounds in up to 95 % yield. Besides, a protocol for [Pt(O^N^C^N)]-catalyzed intramolecular photocyclization of acrylanilides to give structurally diverse 3,4-dihydroquinolinones has been developed.

TMSOTf-mediated synthesis of skipped dienes through the addition of olefins to imines and semicyclicN,O-acetals

A novel approach to skipped dienes has been developed through the TMSOTf-mediated one-pot addition-substitution of olefins2a,2fand2gwith imines1a-1g, and a series of aryl substituted skipped dienes3aa-3gfwere accordingly obtained in 62%-94% yields. Moreov

Synthesis of non-nucleoside anti-viral cyclopropylcarboxacyl hydrazones and initial anti-HSV-1 structure-activity relationship studies

The synthesis of a lead anti-viral cyclopropyl carboxy acyl hydrazone 4F17 (5) and three sequential arrays of structural analogues along with the initial assessment and optimization of the antiviral pharmacophore against the herpes simplex virus type 1 (HSV-1) are reported.