4-(TERT-BUTYLDIMETHYLSILYLOXY) CYCLOHEXANONE

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Reagent Code: #240200
label
Alias 4-(tert-butyldimethylsilyloxy)cyclohexanone; 4-(tert-Butyl-dimethyl-silanyloxy)-cyclohexanone
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CAS Number 55145-45-4

science Other reagents with same CAS 55145-45-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.41 g/mol
Formula C₁₂H₂₄O₂Si
badge Registry Numbers
MDL Number MFCD06411307
thermostat Physical Properties
Boiling Point 85℃/1 mmHg (lit.)
inventory_2 Storage & Handling
Density 0.909 g/ml
Storage Room temperature, inert gas, light-proof

description Product Description

Used as a key intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. Its protected hydroxyl group allows selective reactions at other functional sites, making it valuable in multi-step syntheses. Commonly employed in steroid and terpene derivatization where controlled reactivity and stability are required. Also utilized in the development of chiral compounds due to its ability to maintain stereochemistry during transformations.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,100.00
inventory 5g
10-20 days ฿3,680.00
inventory 25g
10-20 days ฿18,000.00

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4-(TERT-BUTYLDIMETHYLSILYLOXY) CYCLOHEXANONE
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Used as a key intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. Its protected hydroxyl group allows selective reactions at other functional sites, making it valuable in multi-step syntheses. Commonly employed in steroid and terpene derivatization where controlled reactivity and stability are required. Also utilized in the development of chiral compounds due to its ability to maintain stereochemistry during transformations.

Used as a key intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. Its protected hydroxyl group allows selective reactions at other functional sites, making it valuable in multi-step syntheses. Commonly employed in steroid and terpene derivatization where controlled reactivity and stability are required. Also utilized in the development of chiral compounds due to its ability to maintain stereochemistry during transformations.

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