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Merck
CN

455652

Sodium p-toluenesulfinate

95%

Synonym(s):

p-Toluenesulfinic acid sodium salt

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About This Item

Linear Formula:
4-CH3C6H4SO2Na
CAS Number:
Molecular Weight:
178.18
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
212-538-5
MDL number:
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Product Name

Sodium p-toluenesulfinate, 95%

InChI key

KFZUDNZQQCWGKF-UHFFFAOYSA-M

InChI

1S/C7H8O2S.Na/c1-6-2-4-7(5-3-6)10(8)9;/h2-5H,1H3,(H,8,9);/q;+1/p-1

SMILES string

[Na+].Cc1ccc(cc1)S([O-])=O

assay

95%

impurities

<5% water

mp

>300 °C (lit.)

functional group

sulfinic acid

Quality Level

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Efficient and Selective Trimerization of Aryl and Alkyl Isocyanates Catalyzed by Sodium p-Toluenesulfinate in the Presence of TBAI in a Solvent-Free Condition.
Moghaddam FM, et al.
Bulletin of the Chemical Society of Japan, 75(4), 851-852 (2002)
Sodium p-toluenesulfinate/copper (II) acetate in free radical reactions of 5-aryl substituted alkenes.
Wang S-F, et al.
Tetrahedron, 55(8), 2273-2288 (1999)
Sodium p-Toluenesulfinate in Free Radical Reactions.
Chuang C-P.
Synthetic Communications, 23(17), 2371-2380 (1993)
Asymmetric induction in the palladium-catalyzed sulfonylation of allylic sulfinates and acetates with chiral phosphine ligands.
Hiroi K and Makino K.
Chemistry Letters (Jpn), 15(4), 617-620 (1986)
Synthesis of cyanohydrin trimethylsilyl ethers catalyzed by potassium p-toluenesulfinate.
Dekamin MG, et al.
Catalysis Communications, 9(6), 1352-1355 (2008)

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