28358-60-3

Basic information

• Product Name: Benzene, 1,1'-ethenylidenebis[2-methoxy-
• CAS NO: 28358-60-3
• Molecular Formula: C16H16O2
• Molecular Weight: 240.302
• Mol File: 28358-60-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzene, 1,1'-ethenylidenebis[2-methoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,1'-ethenylidenebis[2-methoxy-(28358-60-3)
• EPA Substance Registry System: Benzene, 1,1'-ethenylidenebis[2-methoxy-(28358-60-3)

Safety Data

• Hazardous Substances Data: 28358-60-3(Hazardous Substances Data)

Upstream product

• 13139-86-1 4-methoxyphenyl magnesium bromide 
• 100-42-5 styrene 
• 529-28-2 4-iodoanisol 
• 7664-93-9 sulfuric acid 
• 130073-07-3 1,1-bis-(2-methoxyphenyl)ethanol 
• 64-19-7 acetic acid 
• 141-78-6 ethyl acetate 
• 16750-63-3 2-methoxyphenylmagnesium bromide 

Downstream Products

• 56751-16-7 2,2-Bis(2-methoxyphenyl)propane 
• 130073-35-7 2,2-bis(2-methoxyphenyl)butane 
• 5293-78-7 2,2'-dimethoxytolane 
• 14310-34-0 1,2-bis(2-methoxyphenyl)ethane 
• 6706-92-9 2,2'-dimethoxybenzil 
• 13102-33-5 2,2'-dimethoxybenzophenone 
• 56751-18-9 2,2'-(ethene-1,1-diyl)diphenol 
• 93584-74-8 3,3,6,6-Tetrakis(2-methoxyphenyl)-1,2-dioxane 
• 86927-84-6 4-Methoxy-5-(2-methoxy-phenyl)-11-aza-benzo[a]anthracene-7,12-dione 
• 93404-16-1 4-methoxy-5-(o-methoxyphenyl)naphtho<1,2-g>quinoxaline-7,12-dione 
• 93404-04-7 4-methoxy-5-(o-methoxyphenyl)benzanthracene-7,12-dione 
• 80554-93-4 4-Methoxy-5-(2-methoxy-phenyl)-8-aza-benzo[a]anthracene-7,12-dione 
• 5293-93-6 β,β-bis(o-methoxyphenyl)vinyl bromide 
• 33451-17-1 1,1-bis-(2-methoxy-phenyl)-ethane 

Relevant articles and documents

Effect of immobilization on catalytic characteristics of saturated Pd-N-heterocyclic carbenes in Mizoroki-Heck reactions

A saturated Pd-N-heterocyclic complex was immobilized on an amorphous silica. The complex itself is of very high thermal stability. However, TEM observations, hot filtration, reusability, and poisoning tests all revealed that the complex acted only as a precatalyst to highly active Pd species in Mizoroki-Heck reactions when immobilized. The complex appears more stable when used under homogeneous reaction conditions. The immobilized complex afforded high turnover numbers, 104-105. The higher turnover frequencies were realized at the lower Pd concentrations, which is a characteristic property of ligand-free Pd catalyzed reactions.

Herbicidal 12-substituted 12H-dibenzo(D,G)(1,3)dioxocin-6-carboxylic acids

Dibenzo[d,g][1,3]dioxocin-6-carboxylic acids substituted by methyl or ethyl or a moiety --CH2 CH2 -- at the 12-position and optionally substituted at other positions, such as methyl 4'-chlorospiro(cyclopropane-1,12'(12'H)-dibenzo[d,g][1,3]dioxocin)-6'-carboxylic acid, and their agriculturally acceptable esters, amides, and salts are useful for the control of undesirable vegetation. The 1,1-diarylcyclopropane intermediates required for the spirocyclopropane compounds can be prepared from appropriately substituted 1,1-diarylethene procursors by reaction with phenylthiomethyl lithium reagent.