tert-Butyldiphenylsilyl Trifluoromethanesulfonate

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Reagent Code: #88310
label
Alias tert-Butyldiphenylsilyl trifluoromethanesulfonate;
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CAS Number 92886-86-7

science Other reagents with same CAS 92886-86-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 388.48 g/mol
Formula C₁₇H₁₉F₃O₃SSi
inventory_2 Storage & Handling
Storage 2~8°C, inert gas protection

description Product Description

This chemical is widely used as a protecting group reagent in organic synthesis, particularly for alcohols and phenols. It selectively forms tert-butyldiphenylsilyl (TBDPS) ethers, providing stability under various reaction conditions while allowing for easy deprotection when needed. Its triflate group enhances reactivity, making it effective in silylation reactions. Additionally, it is employed in the synthesis of complex molecules, including natural products and pharmaceuticals, where precise protection and deprotection steps are crucial. Its compatibility with a range of functional groups makes it a versatile tool in multistep synthetic processes.

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Test Parameter Specification
Purity (LC) 96.5-100
Appearance colorless to brown liquid

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿720.00
inventory 5g
10-20 days ฿2,900.00

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tert-Butyldiphenylsilyl Trifluoromethanesulfonate
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This chemical is widely used as a protecting group reagent in organic synthesis, particularly for alcohols and phenols. It selectively forms tert-butyldiphenylsilyl (TBDPS) ethers, providing stability under various reaction conditions while allowing for easy deprotection when needed. Its triflate group enhances reactivity, making it effective in silylation reactions. Additionally, it is employed in the synthesis of complex molecules, including natural products and pharmaceuticals, where precise protectio

This chemical is widely used as a protecting group reagent in organic synthesis, particularly for alcohols and phenols. It selectively forms tert-butyldiphenylsilyl (TBDPS) ethers, providing stability under various reaction conditions while allowing for easy deprotection when needed. Its triflate group enhances reactivity, making it effective in silylation reactions. Additionally, it is employed in the synthesis of complex molecules, including natural products and pharmaceuticals, where precise protection and deprotection steps are crucial. Its compatibility with a range of functional groups makes it a versatile tool in multistep synthetic processes.

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