98582-25-3

Basic information

• Product Name: 1-<(tert-butyldimethylsilyl)oxy>-3-ethenyl-1-cyclohexene
• Synonyms: 1-<(tert-butyldimethylsilyl)oxy>-3-ethenyl-1-cyclohexene
• CAS NO: 98582-25-3
• Molecular Weight: 238.445
• Mol File: 98582-25-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-<(tert-butyldimethylsilyl)oxy>-3-ethenyl-1-cyclohexene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-<(tert-butyldimethylsilyl)oxy>-3-ethenyl-1-cyclohexene(98582-25-3)
• EPA Substance Registry System: 1-<(tert-butyldimethylsilyl)oxy>-3-ethenyl-1-cyclohexene(98582-25-3)

Safety Data

• Hazardous Substances Data: 98582-25-3(Hazardous Substances Data)

Upstream product

• 930-68-7 cyclohexenone 
• 1826-67-1 vinyl magnesium bromide 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 69739-34-0 t-butyldimethylsiyl triflate 

Downstream Products

• 40996-91-6 3-vinyl-cyclohex-2-enone 
• 98582-29-7 1-(tert-Butyl-dimethyl-silanyloxy)-3-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-cyclohexene 
• 108294-13-9 1-<(tert-butyldimethylsilyl)oxy>-3-<2-<(tert-butyldiphenylsilyl)oxy>ethyl>-1-cyclohexene 
• 98582-27-5 2-[3-(tert-Butyl-dimethyl-silanyloxy)-cyclohex-2-enyl]-ethanol 

Relevant articles and documents

Oxidative conversion of silyl enol ethers to α,β-unsaturated ketones employing oxoammonium salts

The oxidative conversion of silyl enol ethers to α,β-unsaturated ketones using a less-hindered class of oxoammonium salts (AZADO +BF4-) is described. The reaction proceeds via the ene-like addition of oxoammonium salts to silyl enol ethers.

Synthesis and 5-lipoxygenase inhibitory activity of 5-hydroperoxy-6,8,11,14-eicosatetraenoic acid analogues

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