Sodium 2, 3-dihydro-1, 4-benzodioXnne-6-sulfinate

95%

Reagent Code: #236547
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CAS Number 1514973-39-7

science Other reagents with same CAS 1514973-39-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.19 g/mol
Formula C₈H₇NaO₄S
badge Registry Numbers
MDL Number MFCD24113278
inventory_2 Storage & Handling
Storage Room temperature, dry, light-proof

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs requiring sulfinate functional groups for their activity. It serves as a key building block in organic reactions, especially in cross-coupling processes where sulfinate salts act as aryl radical precursors. Commonly applied in the preparation of biologically active molecules, including potential antiviral and anti-inflammatory agents. Its stability and reactivity profile make it suitable for use in controlled laboratory-scale reactions aimed at constructing complex aromatic structures.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,090.00
inventory 250mg
10-20 days ฿8,430.00
inventory 1g
10-20 days ฿27,220.00

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Sodium 2, 3-dihydro-1, 4-benzodioXnne-6-sulfinate
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs requiring sulfinate functional groups for their activity. It serves as a key building block in organic reactions, especially in cross-coupling processes where sulfinate salts act as aryl radical precursors. Commonly applied in the preparation of biologically active molecules, including potential antiviral and anti-inflammatory agents. Its stability and reactivity profile make it suitable for use in contr

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs requiring sulfinate functional groups for their activity. It serves as a key building block in organic reactions, especially in cross-coupling processes where sulfinate salts act as aryl radical precursors. Commonly applied in the preparation of biologically active molecules, including potential antiviral and anti-inflammatory agents. Its stability and reactivity profile make it suitable for use in controlled laboratory-scale reactions aimed at constructing complex aromatic structures.

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