1093663-45-6

Basic information

• Product Name: 2,2,3,3,14,14,15,15-octamethyl-11,11-diphenyl-4,13-dioxa-3,14-disilahexadec-8-yn-7-ol
• Synonyms: 2,2,3,3,14,14,15,15-octamethyl-11,11-diphenyl-4,13-dioxa-3,14-disilahexadec-8-yn-7-ol
• CAS NO: 1093663-45-6
• Molecular Weight: 538.918
• Mol File: 1093663-45-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2,2,3,3,14,14,15,15-octamethyl-11,11-diphenyl-4,13-dioxa-3,14-disilahexadec-8-yn-7-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2,3,3,14,14,15,15-octamethyl-11,11-diphenyl-4,13-dioxa-3,14-disilahexadec-8-yn-7-ol(1093663-45-6)
• EPA Substance Registry System: 2,2,3,3,14,14,15,15-octamethyl-11,11-diphenyl-4,13-dioxa-3,14-disilahexadec-8-yn-7-ol(1093663-45-6)

Safety Data

• Hazardous Substances Data: 1093663-45-6(Hazardous Substances Data)

Upstream product

• 22490-19-3 2,2-diphenylpenta-4-yn-1-ol 
• 906542-82-3 methyl 2,2-diphenylpent-4-ynoate 
• 3469-00-9 methyl 2,2-diphenylacetate 
• 1093663-30-9 tert-butyl(2,2-diphenylpent-4-yn-1-yloxy)dimethylsilane 
• 89922-82-7 3-(tert-butyldimethylsilanyloxy)propionaldehyde 

Downstream Products

• 1093662-82-8 7,7-diphenyloct-4-yne-1,3,8-triol 
• 1093662-83-9 3,3-diphenyl-1,6-dioxaspiro[4.5]dec-9-ene 

Relevant articles and documents

Leveraging the micellar effect: Gold-catalyzed dehydrative cyclizations in water at room temperature

The first examples of gold-catalyzed cyclizations of diols and triols to the corresponding hetero- or spirocycles in an aqueous medium are presented. These reactions take place within nanomicelles, where the hydrophobic effect is operating, thereby driving the dehydrations, notwithstanding the surrounding water. By the addition of simple salts such as sodium chloride, reaction times and catalyst loadings can be significantly decreased.