Trifluoromethyl 1,1,2,2,3,3,4,4,4-Nonafluorobutane-1-sulfonate

≥95.0%(GC)

Reagent Code: #238518
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CAS Number 79410-57-4

science Other reagents with same CAS 79410-57-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 368.09 g/mol
Formula C₅F₁₂O₃S
thermostat Physical Properties
Boiling Point 94 °C
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used primarily as a highly reactive sulfonylating agent in organic synthesis, enabling the introduction of sulfonate groups into complex molecules. Its strong electron-withdrawing properties make it especially effective in promoting nucleophilic substitution reactions. Commonly applied in the preparation of pharmaceuticals, agrochemicals, and specialty materials where stable sulfonate esters are required. Also utilized in the development of fluorinated compounds for advanced materials due to its thermal and chemical stability.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿17,870.00
Trifluoromethyl 1,1,2,2,3,3,4,4,4-Nonafluorobutane-1-sulfonate
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Used primarily as a highly reactive sulfonylating agent in organic synthesis, enabling the introduction of sulfonate groups into complex molecules. Its strong electron-withdrawing properties make it especially effective in promoting nucleophilic substitution reactions. Commonly applied in the preparation of pharmaceuticals, agrochemicals, and specialty materials where stable sulfonate esters are required. Also utilized in the development of fluorinated compounds for advanced materials due to its thermal

Used primarily as a highly reactive sulfonylating agent in organic synthesis, enabling the introduction of sulfonate groups into complex molecules. Its strong electron-withdrawing properties make it especially effective in promoting nucleophilic substitution reactions. Commonly applied in the preparation of pharmaceuticals, agrochemicals, and specialty materials where stable sulfonate esters are required. Also utilized in the development of fluorinated compounds for advanced materials due to its thermal and chemical stability.

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