Sodium Pyridine-2-sulfinate

>95%(T)

Reagent Code: #235840
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CAS Number 24367-66-6

science Other reagents with same CAS 24367-66-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 165.1455 g/mol
Formula C₅H₄NNaO₂S
badge Registry Numbers
MDL Number MFCD20483664
thermostat Physical Properties
Melting Point 285 °C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key reagent in organic synthesis, particularly in the preparation of sulfones and sulfoxides through sulfination reactions. It serves as a source of the pyridine-2-sulfinyl group, enabling the introduction of sulfur-containing functionalities into pharmaceutical intermediates and agrochemicals. Its reactivity makes it valuable in radical reactions and transition-metal-catalyzed couplings where controlled sulfur transfer is required. Additionally, it finds use in the development of functional materials and in research laboratories for modifying heterocyclic compounds to enhance biological activity or physicochemical properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,300.00
inventory 250mg
10-20 days ฿9,130.00
inventory 1g
10-20 days ฿24,960.00
Sodium Pyridine-2-sulfinate
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Used as a key reagent in organic synthesis, particularly in the preparation of sulfones and sulfoxides through sulfination reactions. It serves as a source of the pyridine-2-sulfinyl group, enabling the introduction of sulfur-containing functionalities into pharmaceutical intermediates and agrochemicals. Its reactivity makes it valuable in radical reactions and transition-metal-catalyzed couplings where controlled sulfur transfer is required. Additionally, it finds use in the development of functional ma

Used as a key reagent in organic synthesis, particularly in the preparation of sulfones and sulfoxides through sulfination reactions. It serves as a source of the pyridine-2-sulfinyl group, enabling the introduction of sulfur-containing functionalities into pharmaceutical intermediates and agrochemicals. Its reactivity makes it valuable in radical reactions and transition-metal-catalyzed couplings where controlled sulfur transfer is required. Additionally, it finds use in the development of functional materials and in research laboratories for modifying heterocyclic compounds to enhance biological activity or physicochemical properties.

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