tert-butyl(cyclopent-3-en-1-yloxy)diphenylsilane

95%

Reagent Code: #242814
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CAS Number 182801-94-1

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 322.52 g/mol
Formula C₂₁H₂₆OSi
thermostat Physical Properties
Boiling Point 375.5±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.02±0.1 g/cm3(Predicted)
Storage Room temperature

description Product Description

This compound serves as a protected intermediate in organic synthesis, specifically the tert-butyldiphenylsilyl (TBDPS) ether of cyclopent-3-en-1-ol. The bulky TBDPS protecting group shields the hydroxyl functionality, enabling selective manipulations of the cyclopentene moiety, such as additions to the double bond, ring-opening reactions, or further functionalizations. This enhances stability and selectivity in multi-step syntheses, particularly for assembling complex structures like natural products or pharmaceutical intermediates. It is particularly useful in orthogonal protection strategies, allowing deprotection of the silyl group without affecting other functionalities.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿18,420.00
inventory 250mg
10-20 days ฿32,740.00
inventory 1g
10-20 days ฿65,490.00

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tert-butyl(cyclopent-3-en-1-yloxy)diphenylsilane
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This compound serves as a protected intermediate in organic synthesis, specifically the tert-butyldiphenylsilyl (TBDPS) ether of cyclopent-3-en-1-ol. The bulky TBDPS protecting group shields the hydroxyl functionality, enabling selective manipulations of the cyclopentene moiety, such as additions to the double bond, ring-opening reactions, or further functionalizations. This enhances stability and selectivity in multi-step syntheses, particularly for assembling complex structures like natural products or

This compound serves as a protected intermediate in organic synthesis, specifically the tert-butyldiphenylsilyl (TBDPS) ether of cyclopent-3-en-1-ol. The bulky TBDPS protecting group shields the hydroxyl functionality, enabling selective manipulations of the cyclopentene moiety, such as additions to the double bond, ring-opening reactions, or further functionalizations. This enhances stability and selectivity in multi-step syntheses, particularly for assembling complex structures like natural products or pharmaceutical intermediates. It is particularly useful in orthogonal protection strategies, allowing deprotection of the silyl group without affecting other functionalities.

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