51936-06-2

Basic information

• Product Name: Benzene, 1,1'-(2,2-dimethoxyethylidene)bis-
• CAS NO: 51936-06-2
• Molecular Formula: C16H18O2
• Molecular Weight: 242.318
• Mol File: 51936-06-2.mol
• Article Data: 15

Chemical Properties

• CAS DataBase Reference: Benzene, 1,1'-(2,2-dimethoxyethylidene)bis-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,1'-(2,2-dimethoxyethylidene)bis-(51936-06-2)
• EPA Substance Registry System: Benzene, 1,1'-(2,2-dimethoxyethylidene)bis-(51936-06-2)

Safety Data

• Hazardous Substances Data: 51936-06-2(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 947-91-1 Diphenylacetaldehyde 
• 645-49-8 cis-stilben 
• 103-30-0 (E)-1,2-diphenyl-ethene 
• 116117-99-8 1,2-diphenyl-1-methoxy-2-phenylselenenyl ethane dichloride, threo 
• 1689-71-0 cis-1,2-diphenyloxirane 
• 149-73-5 trimethyl orthoformate 
• 1439-07-2 trans-Stilbene oxide 
• 588-59-0 stilbene 
• 119-61-9 benzophenone 
• 530-48-3 1,1-Diphenylethylene 
• 18586-58-8 1,2-bis(trimethylsilyl)-1,2-diphenylethane 
• 40237-72-7 (2-methoxyethene-1,1-diyl)dibenzene 
• 24894-88-0 threo-1,2-diphenyl-1,2-bis(trimethylsilyl)ethane 

Downstream Products

• 40650-77-9 2-methyl-1,4-diphenylnaphthalene 
• 683278-52-6 C₂₁H₂₄I₂O 

Relevant articles and documents

ENOL ETHER PROPERFUME

The present invention relates to compounds of formula (I) as properfume compounds. In particular, the present invention relates to a method to release a compound being a ketone or aldehyde of formula (II), a formate ester of formula (III) and/or an alcoho

Substrate-Dependent Electrochemical Dimethoxylation of Olefins

A general and direct electrochemical dimethoxylation of olefins is reported, which enables a divergent route to different products depending on the structure of olefins. The present protocol features mild conditions and broad substrate scope (49 examples) obviating the usage of transtion-metals and external oxidants. More importantly, to rationalize the divergent route of the transformation, an ionic-like pathway involving carbocation intermediate is proposed and the diverse products is attributed to the different stability of carbocations. (Figure presented.).

Epoxide ring-opening and Meinwald rearrangement reactions of epoxides catalyzed by mesoporous aluminosilicates

Mesoporous aluminosilicates efficiently catalyze the ring-opening of epoxides to produce β-alkoxyalcohols in high yields under extremely mild reaction conditions. These materials also catalyze the corresponding Meinwald rearrangement in non-nucleophilic solvents to give aldehydes which can be trapped in situ to provide the corresponding acetals in an efficient tandem process. The Royal Society of Chemistry 2009.