Di-tert-butylsilyl bis(trifluoromethanesulfonate)

97%

Reagent Code: #97346
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Alias Bis(trifluoromethanesulfonyl)di-tert-butylsilyl ester, di-tert-butylbis(trifluoromethanesulfonyloxy)silane, di-tert-butylsilylbis(trifluoromethanesulfonyl)ester DTBS II (triflate)
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CAS Number 85272-31-7

science Other reagents with same CAS 85272-31-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 440.45 g/mol
Formula C₁₀H₁₈F₆O₆S₂Si
badge Registry Numbers
MDL Number MFCD00010581
thermostat Physical Properties
Boiling Point 73-75 °C0.35 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.352 g/mL at 25 °C(lit.)
Storage room temperature, dry

description Product Description

Used as a highly effective silylating agent in organic synthesis, particularly for protecting hydroxyl groups in complex molecules. Its strong electrophilic nature makes it suitable for activating alcohols and phenols, enabling selective reactions in multi-step synthetic processes. Commonly applied in the preparation of sensitive intermediates in pharmaceutical and fine chemical industries. Also utilized in the synthesis of natural products and polymers, where precise control over functional group transformations is critical. Its stability and reactivity under mild conditions make it a valuable reagent in modern synthetic chemistry.

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Test Parameter Specification
Purity (Titration by NaOH) 96.5-103.5
Purity (GC) 97-100
Refractive Index (n20D) 1.396-1.4
Specific Gravity (2020) 1.354-1.364
Appearance Colorless to yellow liquid
Infrared Spectrum Conforms to Structure
Proton NMR Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿8,360.00
inventory 1g
10-20 days ฿400.00
inventory 250g
10-20 days ฿64,880.00
inventory 100g
10-20 days ฿32,000.00
inventory 5g
10-20 days ฿1,900.00

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Di-tert-butylsilyl bis(trifluoromethanesulfonate)
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Used as a highly effective silylating agent in organic synthesis, particularly for protecting hydroxyl groups in complex molecules. Its strong electrophilic nature makes it suitable for activating alcohols and phenols, enabling selective reactions in multi-step synthetic processes. Commonly applied in the preparation of sensitive intermediates in pharmaceutical and fine chemical industries. Also utilized in the synthesis of natural products and polymers, where precise control over functional group transf

Used as a highly effective silylating agent in organic synthesis, particularly for protecting hydroxyl groups in complex molecules. Its strong electrophilic nature makes it suitable for activating alcohols and phenols, enabling selective reactions in multi-step synthetic processes. Commonly applied in the preparation of sensitive intermediates in pharmaceutical and fine chemical industries. Also utilized in the synthesis of natural products and polymers, where precise control over functional group transformations is critical. Its stability and reactivity under mild conditions make it a valuable reagent in modern synthetic chemistry.

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