121284-44-4

Basic information

• Product Name: Silane, [(1,1-diphenyl-2-propynyl)oxy]trimethyl-
• CAS NO: 121284-44-4
• Molecular Formula: C18H20OSi
• Molecular Weight: 280.442
• Mol File: 121284-44-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Silane, [(1,1-diphenyl-2-propynyl)oxy]trimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Silane, [(1,1-diphenyl-2-propynyl)oxy]trimethyl-(121284-44-4)
• EPA Substance Registry System: Silane, [(1,1-diphenyl-2-propynyl)oxy]trimethyl-(121284-44-4)

Safety Data

• Hazardous Substances Data: 121284-44-4(Hazardous Substances Data)

Upstream product

• 27607-77-8 trimethylsilyl trifluoromethanesulfonate 
• 3923-52-2 1,1-diphenyl-2-propyn-1-ol 
• 119-61-9 benzophenone 
• 1066-54-2 trimethylsilylacetylene 
• 999-97-3 1,1,1,3,3,3-hexamethyl-disilazane 
• 75-77-4 chloro-trimethyl-silane 

Downstream Products

• 1055873-74-9 (8-indan-5-yl-1,1-diphenyloct-4-en-2-ynyloxy)trimethylsilane 
• 1055873-70-5 (E)-(1,1-diphenylundec-4-en-2-ynyloxy)trimethylsilane 
• 1055873-71-6 (E)-8,8-diphenyl-8-trimethylsilanyloxyoct-4-en-6-yn-1-ol 
• 1055873-72-7 (E)-9,9-diphenyl-9-(trimethylsilanyloxy)non-5-en-7-ynoic acid methyl ester 
• 1055873-73-8 (E)-trimethyl-(1,1,5-triphenylpent-4-en-2-ynyloxy)silane 
• 1169859-27-1 2-(diphenyl(trimethylsilyloxy)methyl)fumaronitrile 
• 1169858-90-5 2-(diphenyl(trimethylsilyloxy)methyl)maleonitrile 
• 350693-36-6 1,1-diphenyl-3-(trimethylsilyl)-1-(trimethylsilyloxy)prop-2-yne 
• 3923-52-2 1,1-diphenyl-2-propyn-1-ol 
• 1210-39-5 3,3-diphenyl-2-propenal 
• 105020-24-4 4,4-Diphenyl-1-(2,4,6-tri-t-butylphenyl)-1-phospha-1,2,3-butatriene 
• 1280661-22-4 (E)-9-(5,5-diphenyl-5-(trimethylsiloxy)pent-1-en-3-yn-1-yl)-9H-carbazole 

Relevant articles and documents

Bronsted acid mediated nitrogenation of propargylic alcohols: An efficient approach to alkenyl nitriles

A novel and efficient approach to alkenyl nitriles from readily available propargylic alcohols has been developed. This nitrogenation reaction is transition-metal-free and could be conducted under air at ambient temperature, which makes this protocol promising and practical. Moreover, NH4Br is disclosed as an efficient additive to promote the stereoselectivity of this reaction. the Partner Organisations 2014.

Palladium-catalyzed cyanation of carbon-carbon triple bonds under aerobic conditions

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