365203
Lithium p-toluenesulfinate
98%
Synonym(s):
p-Toluenesulfinic acid lithium salt
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About This Item
Linear Formula:
CH3C6H4SO2Li
CAS Number:
Molecular Weight:
162.14
Beilstein:
4163977
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
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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 Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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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)
P G Righetti et al.
Electrophoresis, 15(8-9), 1005-1013 (1994-08-01)
Potential gravity-induced deformations of polyacrylamide matrices during gelling were investigated in two different initiator systems based on (i) photopolymerization with 100 microM methylene blue, 1 mM sodium toluene sulfinate (reducer) and 50 microM diphenyliodonium chloride (oxidizer) (photopolymerization) and (ii) chemical
Ananda S Amarasekara et al.
Bioresource technology, 125, 114-118 (2012-10-03)
Single step pretreatment-saccharification of corn stover was investigated in aqueous p-toluenesulfonic and sulfuric acid media. Dilute aqueous solution of p-toluenesulfonic acid was a better catalyst than aqueous sulfuric acid of the same H(+) ion concentration for single step pretreatment-saccharification of
Jumat Salimon et al.
Journal of biomedicine & biotechnology, 2011, 196565-196565 (2011-12-02)
For environmental reasons, a new class of environmentally acceptable and renewable biolubricant based on vegetable oils is available. In this study, oxirane ring opening reaction of monoepoxide linoleic acid (MEOA) was done by nucleophilic addition of oleic acid (OA) with
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