(S)-4-((tert-Butyldimethylsilyl)oxy)-5,5-dimethylhexan-2-one

97%

Reagent Code: #232858
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CAS Number 612492-55-4

science Other reagents with same CAS 612492-55-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.4723 g/mol
Formula C₁₄H₃₀O₂Si
thermostat Physical Properties
Boiling Point 280.6±23.0 °C(Predicted)
inventory_2 Storage & Handling
Density 0.863±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of statins such as atorvastatin and rosuvastatin. Its silyl-protected hydroxyl group and ketone functionality allow for selective transformations in multi-step organic syntheses. The stereochemistry enables high enantioselectivity in downstream reactions, making it valuable in asymmetric synthesis. Commonly employed in research and development of active pharmaceutical ingredients (APIs) where precise stereocontrol is required.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,800.00
inventory 250mg
10-20 days ฿14,400.00
inventory 500mg
10-20 days ฿17,600.00
inventory 1g
10-20 days ฿24,000.00
(S)-4-((tert-Butyldimethylsilyl)oxy)-5,5-dimethylhexan-2-one
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Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of statins such as atorvastatin and rosuvastatin. Its silyl-protected hydroxyl group and ketone functionality allow for selective transformations in multi-step organic syntheses. The stereochemistry enables high enantioselectivity in downstream reactions, making it valuable in asymmetric synthesis. Commonly employed in research and development of active pharmaceutical ingredients (APIs) where precise ste

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of statins such as atorvastatin and rosuvastatin. Its silyl-protected hydroxyl group and ketone functionality allow for selective transformations in multi-step organic syntheses. The stereochemistry enables high enantioselectivity in downstream reactions, making it valuable in asymmetric synthesis. Commonly employed in research and development of active pharmaceutical ingredients (APIs) where precise stereocontrol is required.

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