| Weight | 118.089 g/mol |
|---|---|
| Formula | CH3NaO3S |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
Sodium hydroxymethanesulfinate (149-44-0)
Rongalite · formaldehydesulfoxylate · sodium formaldehydesulfoxylate
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- Nanosized silver powder via reduction of silver nitrate by sodium formaldehydesulfoxylate in acidic pH medium (Materials Letters, 2003)
- Rongalite: a useful green reagent in organic synthesis. (Chemical Reviews, 2012)
- Rongalite promoted highly regioselective synthesis of -hydroxy sulfides by ring opening of epoxides with disulfides (Tetrahedron, 2009)
- A new odorless one-pot synthesis of thioesters and selenoesters promoted by Rongalite (Tetrahedron, 2010)
- Design and Synthesis of Benzosultine-sulfone as a o-Xylylene Precursor via Cross-enyne Metathesis and Rongalite: Further Expansion to Polycyclics via Regioselective DielsAlder Reaction (Journal of Organic Chemistry, 2010)
- Differential reactivity pattern of hybrid o-quinodimethane precursors: strategic expansion to annulated benzocycloalkanes via rongalite (Journal of Organic Chemistry, 2009)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Rongalite
- formaldehydesulfoxylate
- sodium formaldehydesulfoxylate
- formaldehydesulfoxylate, magnesium (2:1) salt
- formaldehydesulfoxylate, monosodium salt
- formaldehydesulfoxylate dihydrate
-
SMILESC(O)S(=O)[O-].[Na+]
-
InChIKeyXWGJFPHUCFXLBL-UHFFFAOYSA-M
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Sodium hydroxymethanesulfinate
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