Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | CH4O3S |
| Molecular Weight | 96.106 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OCS(O)=O
InChI
InChIKey=SBGKURINHGJRFN-UHFFFAOYSA-N
InChI=1S/CH4O3S/c2-1-5(3)4/h2H,1H2,(H,3,4)
| Molecular Formula | CH4O3S |
| Molecular Weight | 96.106 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
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 |
|---|---|---|
| Isotachophoretic determination of hydrosulfite and metabisulfite in technical samples. | 2007 Nov 30 |
|
| Differential reactivity pattern of hybrid o-quinodimethane precursors: strategic expansion to annulated benzocycloalkanes via rongalite. | 2009 Aug 7 |
|
| 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 Jun 18 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:20:51 UTC 2023
by
admin
on
Fri Dec 15 16:20:51 UTC 2023
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| Record UNII |
M049N73196
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| Record Status |
Validated (UNII)
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| Record Version |
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SALT/SOLVATE -> PARENT | |||
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SALT/SOLVATE -> PARENT | |||
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SALT/SOLVATE -> PARENT |
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ACTIVE MOIETY |
