Sodium 5, 6, 7, 8-tetrahydronaphthalene-2-sulfinate

95%

Reagent Code: #236546
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CAS Number 1504174-30-4

science Other reagents with same CAS 1504174-30-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.25 g/mol
Formula C₁₀H₁₁NaO₂S
badge Registry Numbers
MDL Number MFCD24113300
inventory_2 Storage & Handling
Storage Room temperature, dry, light-proof

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of biologically active compounds and pharmaceuticals. Its sulfinate group allows for sulfur-based transformations, making it valuable in the development of sulfone or sulfonamide derivatives. It also serves in research settings for studying reaction mechanisms involving radical or nucleophilic pathways. Due to its reactive nature, it is employed in controlled environments to build complex aromatic and partially saturated ring systems for drug discovery and material science applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,980.00
inventory 250mg
10-20 days ฿15,960.00
inventory 1g
10-20 days ฿50,040.00
Sodium 5, 6, 7, 8-tetrahydronaphthalene-2-sulfinate
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Used as an intermediate in organic synthesis, particularly in the preparation of biologically active compounds and pharmaceuticals. Its sulfinate group allows for sulfur-based transformations, making it valuable in the development of sulfone or sulfonamide derivatives. It also serves in research settings for studying reaction mechanisms involving radical or nucleophilic pathways. Due to its reactive nature, it is employed in controlled environments to build complex aromatic and partially saturated ring s

Used as an intermediate in organic synthesis, particularly in the preparation of biologically active compounds and pharmaceuticals. Its sulfinate group allows for sulfur-based transformations, making it valuable in the development of sulfone or sulfonamide derivatives. It also serves in research settings for studying reaction mechanisms involving radical or nucleophilic pathways. Due to its reactive nature, it is employed in controlled environments to build complex aromatic and partially saturated ring systems for drug discovery and material science applications.

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