125055-91-6

Basic information

• Product Name: 4,4′-(2-(4-chlorophenyl)ethene-1,1-diyl)bis(methoxybenzene)
• Synonyms: 4,4′-(2-(4-chlorophenyl)ethene-1,1-diyl)bis(methoxybenzene)
• CAS NO: 125055-91-6
• Molecular Weight: 350.845
• Mol File: 125055-91-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 4,4′-(2-(4-chlorophenyl)ethene-1,1-diyl)bis(methoxybenzene)(CAS DataBase Reference)
• NIST Chemistry Reference: 4,4′-(2-(4-chlorophenyl)ethene-1,1-diyl)bis(methoxybenzene)(125055-91-6)
• EPA Substance Registry System: 4,4′-(2-(4-chlorophenyl)ethene-1,1-diyl)bis(methoxybenzene)(125055-91-6)

Safety Data

• Hazardous Substances Data: 125055-91-6(Hazardous Substances Data)

Upstream product

• 90-96-0 bis(p-methoxyphenyl)methanone 
• 873-76-7 para-Chlorobenzyl alcohol 
• 127349-06-8 N′-(bis(4-methoxyphenyl)-methylene)-4-methylbenzenesulfonohydrazide 
• 95458-82-5 diethyl 4-chlorobenzyl phosphate 
• 123-11-5 4-methoxy-benzaldehyde 
• 100-66-3 methoxybenzene 
• 104-88-1 4-chlorobenzaldehyde 
• 154544-66-8 diethyl phosphonate 
• 5720-07-0 4-methoxyphenylboronic acid 
• 77295-59-1 1-chloro-4-(2,2-dibromovinyl)benzene 
• 125055-89-2 3-(4-Chloro-phenyl)-2,2-bis-(4-methoxy-phenyl)-thiirane 
• 856373-02-9 2-(4-chloro-phenyl)-1,1-bis-(4-methoxy-phenyl)-ethanol 

Relevant articles and documents

AMINIUM RADICAL SALT CATALYZED DESULPHURIZATION OF THIIRANES: AN EFFICIENT PREPARATION OF ARYLSUBSTITUTED OLEFINS

Arylsubstituted olefins are obtained from corresponding thiiranes in high yields under mild conditions by using catalytic amount of tris-(p-bromophenyl)aminium hexachloroantimonate (1) as a single electron transfer (SET) oxidant.

One-Pot, Three-Component Approach to Diarylmethylphosphonates: A Direct Entry to Polycyclic Aromatic Systems

A new type of three-component reaction was developed consisting of aldehydes, electron-rich (hetero)arenes, and trialkyl phosphite, which provided facile access to a wide range of diarylmethylphosphonates under mild reaction conditions. Simple one- or two-step synthetic manipulation of the resulting compounds enabled us to reach several polycyclic (hetero)aromatic systems efficiently.