1351685-22-7

Basic information

• Product Name: C₃₂H₃₈O₁₂
• Synonyms: C₃₂H₃₈O₁₂
• CAS NO: 1351685-22-7
• Molecular Weight: 614.647
• Mol File: 1351685-22-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₃₂H₃₈O₁₂(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₂H₃₈O₁₂(1351685-22-7)
• EPA Substance Registry System: C₃₂H₃₈O₁₂(1351685-22-7)

Safety Data

• Hazardous Substances Data: 1351685-22-7(Hazardous Substances Data)

Upstream product

• 112-27-6 2,2'-[1,2-ethanediylbis(oxy)]bisethanol 
• 240797-46-0 1,2-bis{2-[2-(2-tosylethoxy)ethoxy]ethoxy}benzene 
• 221002-03-5 4-hydroxymethyldibenzo-24-crown-8 ether 
• 220589-91-3 2-carbomethoxy-dibenzo-24-crown-8 
• 77544-68-4 8-tosyloxy-3,6-dioxaoctanol 
• 88037-68-7 1,2-bis{2-[2-(2-hydroxyethoxy)ethoxy]ethoxy}benzene 
• 1357288-06-2 C₃₈H₄₆O₁₂ 

Relevant articles and documents

Controlled reversible anchoring of η6-arene/TsDPEN- ruthenium(II) complex onto magnetic nanoparticles: A new strategy for catalyst separation and recycling

A new catalyst separation and recycling protocol combining magnetic nanoparticles and host-guest assembly was developed. The catalyst, (η6-arene)[N-(para-toluenesulfonyl)-1,2-diphenylethylenediamine] ruthenium trifluoromethanesulfonate [Ru(OTf)(TsDPEN)(η6-arene)] bearing a dialkylammonium salt tag, was easily separated from the reaction mixtures by magnet-assisted decantation, on basis of the formation of a pseudorotaxane complex by using dibenzo[24]crown-8-modified Fe3O 4 nanoparticles. The ruthenium catalyst has been successfully reused at least 5 times with the retention of enantioselectivity but at the expense of relatively low catalytic activities in the asymmetric hydrogenation of 2-methylquinoline. Copyright