Sodium 2,5-dichlorothiophene-3-sulfinate

95%

Reagent Code: #237607
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CAS Number 363179-59-3

science Other reagents with same CAS 363179-59-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 239.078 g/mol
Formula C₄HCl₂NaO₂S₂
thermostat Physical Properties
Melting Point 266-270 °C
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used primarily as a key intermediate in the synthesis of chlorinated thiophene derivatives, which are important building blocks in the development of pharmaceuticals and agrochemicals. It serves as a chlorinating and sulfination agent in organic reactions, enabling selective functionalization of heterocyclic compounds. Its reactivity makes it valuable in the preparation of active ingredients in crop protection agents and medicinal chemistry, particularly in routes requiring mild sulfinate-based transformations. Also employed in research settings for developing novel conductive polymers and functional materials due to the thiophene backbone’s electronic properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,600.00
inventory 1g
10-20 days ฿6,720.00
inventory 5g
10-20 days ฿24,530.00
Sodium 2,5-dichlorothiophene-3-sulfinate
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Used primarily as a key intermediate in the synthesis of chlorinated thiophene derivatives, which are important building blocks in the development of pharmaceuticals and agrochemicals. It serves as a chlorinating and sulfination agent in organic reactions, enabling selective functionalization of heterocyclic compounds. Its reactivity makes it valuable in the preparation of active ingredients in crop protection agents and medicinal chemistry, particularly in routes requiring mild sulfinate-based transform

Used primarily as a key intermediate in the synthesis of chlorinated thiophene derivatives, which are important building blocks in the development of pharmaceuticals and agrochemicals. It serves as a chlorinating and sulfination agent in organic reactions, enabling selective functionalization of heterocyclic compounds. Its reactivity makes it valuable in the preparation of active ingredients in crop protection agents and medicinal chemistry, particularly in routes requiring mild sulfinate-based transformations. Also employed in research settings for developing novel conductive polymers and functional materials due to the thiophene backbone’s electronic properties.

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