Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | CH3O3S.Na.2H2O |
| Molecular Weight | 154.118 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O.O.[Na+].OCS([O-])=O
InChI
InChIKey=UCWBKJOCRGQBNW-UHFFFAOYSA-M
InChI=1S/CH4O3S.Na.2H2O/c2-1-5(3)4;;;/h2H,1H2,(H,3,4);;2*1H2/q;+1;;/p-1
Hydroxymethanesulfinic acid is an organic acid. Sodium salt of hydroxymethanesulfinic acid (rongalite) is widely used in organic synthesis. It can be used as a reducing agent for elemental selenium and tellurium, diselenides, α‐halo ketones, and aromatic aldehydes; yields symmetrical sulfones with primary halides and with Michael acceptors.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Design and synthesis of benzosultine-sulfone as a o-xylylene precursor via cross-enyne metathesis and rongalite: further expansion to polycyclics via regioselective Diels-Alder reaction. | 2010-06-18 |
|
| Differential reactivity pattern of hybrid o-quinodimethane precursors: strategic expansion to annulated benzocycloalkanes via rongalite. | 2009-08-07 |
|
| Isotachophoretic determination of hydrosulfite and metabisulfite in technical samples. | 2007-11-30 |
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PARENT (SALT/SOLVATE)
SUBSTANCE RECORD