1-(Trimethylsilyloxy)cyclohexene

98.0%(GC)

Reagent Code: #241053
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CAS Number 6651-36-1

science Other reagents with same CAS 6651-36-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 170.33 g/mol
Formula C₉H₁₈OSi
badge Registry Numbers
MDL Number MFCD00001541
thermostat Physical Properties
Boiling Point 165°C(lit.)
inventory_2 Storage & Handling
Density 0.89g/mL
Storage Room temperature, dryness, inert gas storage

description Product Description

Used as a silyl enol ether in organic synthesis, particularly in Mukaiyama aldol reactions where it acts as a nucleophilic enolate equivalent. It is valuable for forming carbon-carbon bonds under mild, Lewis acid-catalyzed conditions. Commonly employed in the synthesis of complex molecules such as natural products and pharmaceuticals due to its stability and reactivity profile. Also serves as a protecting group reagent for enolizable carbonyl compounds during multistep syntheses.

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Size Availability Unit Price Quantity
inventory 5mL
10-20 days ฿950.00
inventory 25ml
10-20 days ฿3,200.00

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1-(Trimethylsilyloxy)cyclohexene
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Used as a silyl enol ether in organic synthesis, particularly in Mukaiyama aldol reactions where it acts as a nucleophilic enolate equivalent. It is valuable for forming carbon-carbon bonds under mild, Lewis acid-catalyzed conditions. Commonly employed in the synthesis of complex molecules such as natural products and pharmaceuticals due to its stability and reactivity profile. Also serves as a protecting group reagent for enolizable carbonyl compounds during multistep syntheses.

Used as a silyl enol ether in organic synthesis, particularly in Mukaiyama aldol reactions where it acts as a nucleophilic enolate equivalent. It is valuable for forming carbon-carbon bonds under mild, Lewis acid-catalyzed conditions. Commonly employed in the synthesis of complex molecules such as natural products and pharmaceuticals due to its stability and reactivity profile. Also serves as a protecting group reagent for enolizable carbonyl compounds during multistep syntheses.

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