70592-04-0

Basic information

• Product Name: (Z)-1,2-bis(4-methoxyphenyl)-1,2-diphenylethylene
• Synonyms: (Z)-1,2-bis(4-methoxyphenyl)-1,2-diphenylethylene
• CAS NO: 70592-04-0
• Molecular Weight: 392.497
• Mol File: 70592-04-0.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: (Z)-1,2-bis(4-methoxyphenyl)-1,2-diphenylethylene(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-1,2-bis(4-methoxyphenyl)-1,2-diphenylethylene(70592-04-0)
• EPA Substance Registry System: (Z)-1,2-bis(4-methoxyphenyl)-1,2-diphenylethylene(70592-04-0)

Safety Data

• Hazardous Substances Data: 70592-04-0(Hazardous Substances Data)

Upstream product

• 611-94-9 4-Methoxybenzophenone 
• 70592-03-9 trans-1,2-di(4-methoxyphenyl)-1,2-diphenylethylene 
• 696-62-8 para-iodoanisole 
• 151416-94-3 (Z)-2,2'-[1,2-(biphenyl)eth-1-ene-1,2-diyl]bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolane) 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 221006-76-4 1,2-bis(pinacolatoboryl)-1,2-diphenylethene 
• 501-65-5 diphenyl acetylene 
• 13139-86-1 4-methoxyphenyl magnesium bromide 
• 5720-07-0 4-methoxyphenylboronic acid 

Downstream Products

• 70592-03-9 trans-1,2-di(4-methoxyphenyl)-1,2-diphenylethylene 
• 343960-74-7 (Z)-4,4'-(1,2-diphenylethene-1,2-diyl)diphenol 

Relevant articles and documents

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

Nickel-catalyzed three-component domino reactions of aryl grignard reagents, alkynes, and aryl halides producing tetrasubstituted alkenes

Three-component reaction of aryl Grignard reagents, alkynes, and aryl halides in the presence of 1 mol % of NiCl2 proceeded sequentially through carbomagnesiation of the alkyne followed by cross-coupling of the resulting alkenyl Grignard reagent with aryl halide to give tetrasubstituted alkenes in high yields.

A heterobimetallic complex featuring a Ti-Co multiple bond and its application to the reductive coupling of ketones to alkenes

To explore metal-metal multiple bonds between first row transition metals, Ti/Co complexes supported by two phosphinoamide ligands have been synthesized and characterized. The Ti metalloligand Cl2Ti(XylNPiPr2)2 (1) was treated with CoI2 under reducing conditions, permitting isolation of the Ti/Co complex [(μ-Cl)Ti(XylNPiPr2)2CoI]2 (2). One electron reduction of complex 2 affords ClTi(XylNPiPr2)2CoPMe3 (3), which features a metal-metal triple bond and an unprecedentedly short Ti-Co distance of 2.0236(9) ?. This complex is shown to promote the McMurry coupling reaction of aryl ketones into alkenes, with concomitant formation of the tetranuclear complex [Ti(μ3-O)(NXylPiPr2)2CoI]2 (4). A cooperative mechanism involving bimetallic C=O bond activation and a cobalt carbene intermediate is proposed.