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Merck

433063

Sigma-Aldrich

Sodium methanesulfinate

technical grade, 85%

Sinónimos:

Methanesulfinic acid sodium salt

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About This Item

Fórmula lineal:
CH3SO2Na
Número de CAS:
Peso molecular:
102.09
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

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

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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.

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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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)
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
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)
Metal-Free Direct Construction of Sulfonamides via Iodine-Mediated Coupling Reaction of Sodium Sulfinates and Amines at Room Temperature.
Wei W, et al.
Advanced Synthesis & Catalysis, 357(5), 987-992 (2015)
S Fukui et al.
Journal of chromatography, 630(1-2), 187-193 (1993-02-05)
For the determination of hydroxyl radicals, dimethyl sulphoxide was used as a molecular probe and the methanesulphinic acid produced was determined by high-performance liquid chromatography of its Fast Yellow GC salt derivative. The results for hydroxyl radicals formed using the

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