4-(((tert-Butyldimethylsilyl)oxy)methyl)cyclohexan-1-ol

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Reagent Code: #130433
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CAS Number 117107-08-1

science Other reagents with same CAS 117107-08-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.45 g/mol
Formula C₁₃H₂₈O₂Si
badge Registry Numbers
MDL Number MFCD28063759
thermostat Physical Properties
Boiling Point 284.3±13.0 °C(Predicted)
inventory_2 Storage & Handling
Density 0.920±0.06 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used primarily as a protected diol intermediate in organic synthesis, particularly in the construction of complex natural products and pharmaceuticals. The silyl ether group provides stability under a variety of reaction conditions while allowing selective deprotection when needed. Its cyclohexanol core with a pendant protected hydroxymethyl group makes it valuable in stereoselective synthesis, where controlled functionalization is required. Commonly employed in multi-step syntheses involving glycosidation, macrolide formation, or polyketide-like structures due to its ability to direct stereochemistry and support carbon chain elongation.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿8,350.00
inventory 1g
10-20 days ฿22,550.00

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4-(((tert-Butyldimethylsilyl)oxy)methyl)cyclohexan-1-ol
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Used primarily as a protected diol intermediate in organic synthesis, particularly in the construction of complex natural products and pharmaceuticals. The silyl ether group provides stability under a variety of reaction conditions while allowing selective deprotection when needed. Its cyclohexanol core with a pendant protected hydroxymethyl group makes it valuable in stereoselective synthesis, where controlled functionalization is required. Commonly employed in multi-step syntheses involving glycosidati

Used primarily as a protected diol intermediate in organic synthesis, particularly in the construction of complex natural products and pharmaceuticals. The silyl ether group provides stability under a variety of reaction conditions while allowing selective deprotection when needed. Its cyclohexanol core with a pendant protected hydroxymethyl group makes it valuable in stereoselective synthesis, where controlled functionalization is required. Commonly employed in multi-step syntheses involving glycosidation, macrolide formation, or polyketide-like structures due to its ability to direct stereochemistry and support carbon chain elongation.

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