Sodium 2, 3-dihydro-1h-indene-5-sulfinate

95%

Reagent Code: #236548
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CAS Number 153261-83-7

science Other reagents with same CAS 153261-83-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 204.22 g/mol
Formula C₉H₉NaO₂S
badge Registry Numbers
MDL Number MFCD24113302
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 pharmaceuticals and fine chemicals. It serves as a sulfinate reagent in cross-coupling reactions, enabling the formation of carbon-sulfur bonds. Its structure allows for functionalization of aromatic systems, making it valuable in the development of bioactive molecules and sulfone-containing compounds. Commonly employed in research settings for the synthesis of indene-based derivatives with potential therapeutic activity.

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Test Parameter Specification
Appearance Solid
Purity (%) 94.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,100.00
inventory 250mg
10-20 days ฿5,140.00
inventory 1g
10-20 days ฿16,560.00

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Sodium 2, 3-dihydro-1h-indene-5-sulfinate
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. It serves as a sulfinate reagent in cross-coupling reactions, enabling the formation of carbon-sulfur bonds. Its structure allows for functionalization of aromatic systems, making it valuable in the development of bioactive molecules and sulfone-containing compounds. Commonly employed in research settings for the synthesis of indene-based derivatives with potential therapeutic activity.

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. It serves as a sulfinate reagent in cross-coupling reactions, enabling the formation of carbon-sulfur bonds. Its structure allows for functionalization of aromatic systems, making it valuable in the development of bioactive molecules and sulfone-containing compounds. Commonly employed in research settings for the synthesis of indene-based derivatives with potential therapeutic activity.

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