Sodium Benzenesulfinate Dihydrate

≥98%

Reagent Code: #234777
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CAS Number 25932-11-0

science Other reagents with same CAS 25932-11-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 164.15 g/mol
Formula C₆H₅NaO₂S·₂H₂O
badge Registry Numbers
MDL Number MFCD00149638
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of sulfones and sulfonamides through reactions with electrophiles or oxidizing agents. It serves as a source of the phenylsulfonyl anion in substitution reactions, enabling the introduction of phenylsulfonyl groups into target molecules. Commonly applied in pharmaceutical synthesis for building active ingredients that require sulfonyl-containing structures. Also utilized in polymer chemistry as a modifier or catalyst in certain radical reactions. Additionally, employed in photochemistry and photocatalysis, functioning as a radical source under light irradiation, with potential in light-controlled reaction acceleration systems. Its stability and solubility in polar solvents make it suitable for use in aqueous and mixed solvent systems.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿260.00
inventory 100g
10-20 days ฿360.00
inventory 500g
10-20 days ฿1,220.00

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Sodium Benzenesulfinate Dihydrate
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Used as a key intermediate in organic synthesis, particularly in the preparation of sulfones and sulfonamides through reactions with electrophiles or oxidizing agents. It serves as a source of the phenylsulfonyl anion in substitution reactions, enabling the introduction of phenylsulfonyl groups into target molecules. Commonly applied in pharmaceutical synthesis for building active ingredients that require sulfonyl-containing structures. Also utilized in polymer chemistry as a modifier or catalyst in cert

Used as a key intermediate in organic synthesis, particularly in the preparation of sulfones and sulfonamides through reactions with electrophiles or oxidizing agents. It serves as a source of the phenylsulfonyl anion in substitution reactions, enabling the introduction of phenylsulfonyl groups into target molecules. Commonly applied in pharmaceutical synthesis for building active ingredients that require sulfonyl-containing structures. Also utilized in polymer chemistry as a modifier or catalyst in certain radical reactions. Additionally, employed in photochemistry and photocatalysis, functioning as a radical source under light irradiation, with potential in light-controlled reaction acceleration systems. Its stability and solubility in polar solvents make it suitable for use in aqueous and mixed solvent systems.

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