433063
Sodium methanesulfinate
technical grade, 85%
Synonym(s):
Methanesulfinic acid sodium salt
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About This Item
Linear Formula:
CH3SO2Na
CAS Number:
Molecular Weight:
102.09
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
243-669-6
MDL number:
Assay:
85%
grade
technical grade
Quality Level
assay
85%
mp
222-226 °C (dec.) (lit.)
functional group
sulfinic acid
SMILES string
[Na+].CS([O-])=O
InChI
1S/CH4O2S.Na/c1-4(2)3;/h1H3,(H,2,3);/q;+1/p-1
InChI key
LYPGDCWPTHTUDO-UHFFFAOYSA-M
Related Categories
General description
Sodium methanesulfinate is an aliphatic sodium sulfinate. Conjugate addition of sodium methanesulfinate to vinyl heterocycles has been described. Cross-coupling reaction between aryl boronic acid and sodium methanesulfinate has been studied. Its stock solution was prepared from methanesulfonic acid by adding one equivalent of sodium hydroxide and diluting it to 4M.
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R Bruck et al.
Journal of hepatology, 35(4), 457-464 (2001-10-30)
Reactive oxygen species and oxidative stress were implicated in hepatic stellate cell activation and liver fibrosis. The aim of the present study was to examine whether the administration of free radical scavengers in vivo would prevent experimentally-induced hepatic cirrhosis in
Design, Synthesis and Discovery of 1-(2-(6-Chloro-3-methylsulfonyl)-naphthyl)-1H-pyrazole-5-carboxylamides as Highly Potent Factor Xa Inhibitors.
Jia ZJ, et al.
Chemical & Pharmaceutical Bulletin, 57(9), 1004-1007 (2009)
A mild and efficient new synthesis of aryl sulfones from boronic acids and sulfinic acid salts.
Beaulieu C, et al.
Tetrahedron Letters, 45(16), 3233-3236 (2004)
Isa G J de Avellar et al.
Biochimica et biophysica acta, 1675(1-3), 46-53 (2004-11-13)
It is widely believed that the iron chelator 1,10-phenanthroline (phen) is able to fully block the Fenton reaction by forming a complex (Fe(phen)3(2+), also known as ferroin) that cannot react with H2O2. We observed that phen cannot fully prevent 2-deoxyribose
Iodine-Catalyzed Oxidative Amination of Sodium Sulfinates: A Convenient Approach to the Synthesis of Sulfonamides under Mild Conditions.
Buathongjan C, et al.
European Journal of Organic Chemistry, 2015(7), 1575-1582 (2015)
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