365203
Lithium p-toluenesulfinate
98%
Sinónimos:
p-Toluenesulfinic acid lithium salt
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About This Item
Fórmula lineal:
CH3C6H4SO2Li
Número de CAS:
Peso molecular:
162.14
Beilstein/REAXYS Number:
4163977
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
Productos recomendados
assay
98%
impurities
≤2% Li2CO3
SMILES string
[Li+].Cc1ccc(cc1)S([O-])=O
InChI
1S/C7H8O2S.Li/c1-6-2-4-7(5-3-6)10(8)9;/h2-5H,1H3,(H,8,9);/q;+1/p-1
InChI key
MSUZXYWQEDRGFN-UHFFFAOYSA-M
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Application
Lithium p-toluenesulfinate may be used in the preparation of 2-oxo-1,3-diphenyl-1,2-dihydroquinoline-4-carbonitrile. It may be used in the preparation of highly fluorescent compound, 3-amino-6-methoxy-4-p-tolylsulfonylquinolone.
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Month 2013 6-Methoxy-2-oxo-1, 2-dihydroquinoline-3, 4-dicarbonitriles, A Red Compound Class with Solvent and pH Independent Green Fluorescence Maxima.
Enoua GC, et al.
Journal of Heterocyclic Chemistry, 51, 492-501 (2014)
4-Cyano-6, 7-dimethoxycarbostyrils with Solvent-and pH-Independent High Fluorescence Quantum Yields and Emission Maxima.
Ahvale AB, et al.
European Journal of Organic Chemistry, 3, 563-571 (2008)
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Journal of chromatography. A, 1129(1), 21-28 (2006-08-09)
Addition of long-chain polyunsaturated fatty acids (LC-PUFAs) from marine oil into food products implies preliminary refining procedures of the oil which thermal process affects the integrity of LC-PUFAs. Deodorization, the major step involving high temperatures, is a common process used
Pierluigi Delmonte et al.
Journal of chromatography. A, 1214(1-2), 30-36 (2008-11-14)
In recent years, several countries have implemented new regulations regarding limitations or labeling of the trans fatty acid (tFA) content in foods. In order to comply with the new requirements, gas chromatographic methods for fatty acid (FA) analysis have been
Shirin Safaei et al.
Molecular diversity, 16(3), 591-600 (2012-08-29)
A variety of pyrazolo[3,4-d]pyrimidine-6(7H)-thione derivatives were easily synthesized with a novel, simple, efficient, and regioselective method via three-component condensation reaction of 5-methyl-1H-pyrazol-3-amine, arylisothiocyanates, and aldehydes in the presence of catalytic amount of p-toluenesulfonic acid (p-TSA) in 1-butyl-3-methylimidazolium bromide ionic liquid
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