Sodium 5-(Trifluoromethyl)pyridine-2-sulfinate

>98%(LC&T)

Reagent Code: #235843
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CAS Number 2098851-48-8

science Other reagents with same CAS 2098851-48-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.1435 g/mol
Formula C₆H₃F₃NNaO₂S
badge Registry Numbers
MDL Number MFCD31442692
thermostat Physical Properties
Melting Point 340 °C (dec)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key reagent in organic synthesis, particularly in trifluoromethylation reactions. It serves as a stable and efficient source of CF3 radicals under mild conditions, enabling the introduction of trifluoromethyl groups into various organic molecules. This is highly valuable in pharmaceutical and agrochemical industries, where trifluoromethylated compounds often exhibit enhanced metabolic stability, lipophilicity, and bioavailability. It is especially useful in transition-metal-free reactions, making processes more cost-effective and environmentally favorable. Its solubility in polar solvents and good shelf stability further support its use in large-scale industrial applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,410.00
inventory 250mg
10-20 days ฿3,250.00
inventory 1g
10-20 days ฿12,970.00
Sodium 5-(Trifluoromethyl)pyridine-2-sulfinate
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Used as a key reagent in organic synthesis, particularly in trifluoromethylation reactions. It serves as a stable and efficient source of CF3 radicals under mild conditions, enabling the introduction of trifluoromethyl groups into various organic molecules. This is highly valuable in pharmaceutical and agrochemical industries, where trifluoromethylated compounds often exhibit enhanced metabolic stability, lipophilicity, and bioavailability. It is especially useful in transition-metal-free reactions, maki

Used as a key reagent in organic synthesis, particularly in trifluoromethylation reactions. It serves as a stable and efficient source of CF3 radicals under mild conditions, enabling the introduction of trifluoromethyl groups into various organic molecules. This is highly valuable in pharmaceutical and agrochemical industries, where trifluoromethylated compounds often exhibit enhanced metabolic stability, lipophilicity, and bioavailability. It is especially useful in transition-metal-free reactions, making processes more cost-effective and environmentally favorable. Its solubility in polar solvents and good shelf stability further support its use in large-scale industrial applications.

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