Triisopropylsilyl trifluoromethanesulfonate

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Reagent Code: #240095
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Alias Triisopropylsilyltrifluoromethanesulfonate
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CAS Number 80522-42-5

science Other reagents with same CAS 80522-42-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 306.42 g/mol
Formula C₁₀H₂₁F₃O₃SSi
badge Registry Numbers
MDL Number MFCD00009913
thermostat Physical Properties
Boiling Point 45-46 °C/0.03 mmHg
inventory_2 Storage & Handling
Density 1.14 g/mL
Storage Room temperature, inert gas atmosphere, drying

description Product Description

Used as a silylating agent in organic synthesis, particularly for the protection of hydroxyl groups in complex molecule assembly. Its bulky triisopropylsilyl group provides high steric shielding, making it effective for selective protection in polyfunctional molecules such as carbohydrates, nucleosides, and natural products. The triflate leaving group enhances reactivity, allowing silylation under mild conditions. Commonly employed in pharmaceutical and agrochemical synthesis where precise functional group control is required. Also used in the preparation of silyl enol ethers and other silicon-based intermediates for carbon–carbon bond formation.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿162.00
inventory 5g
10-20 days ฿300.00
inventory 25g
10-20 days ฿670.00
inventory 100g
10-20 days ฿2,140.00
inventory 500g
10-20 days ฿10,350.00
Triisopropylsilyl trifluoromethanesulfonate
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Used as a silylating agent in organic synthesis, particularly for the protection of hydroxyl groups in complex molecule assembly. Its bulky triisopropylsilyl group provides high steric shielding, making it effective for selective protection in polyfunctional molecules such as carbohydrates, nucleosides, and natural products. The triflate leaving group enhances reactivity, allowing silylation under mild conditions. Commonly employed in pharmaceutical and agrochemical synthesis where precise functional gro

Used as a silylating agent in organic synthesis, particularly for the protection of hydroxyl groups in complex molecule assembly. Its bulky triisopropylsilyl group provides high steric shielding, making it effective for selective protection in polyfunctional molecules such as carbohydrates, nucleosides, and natural products. The triflate leaving group enhances reactivity, allowing silylation under mild conditions. Commonly employed in pharmaceutical and agrochemical synthesis where precise functional group control is required. Also used in the preparation of silyl enol ethers and other silicon-based intermediates for carbon–carbon bond formation.

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