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Merck

365203

Sigma-Aldrich

对甲苯亚磺酸锂

98%

别名:

对甲苯亚磺酸 锂盐

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About This Item

线性分子式:
CH3C6H4SO2Li
CAS号:
分子量:
162.14
Beilstein:
4163977
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:

化驗

98%

雜質

≤2% Li2CO3

SMILES 字串

[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 密鑰

MSUZXYWQEDRGFN-UHFFFAOYSA-M

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應用

Lithium p-toluenesulfinate may be used in the preparation of 2-oxo-1,3-diphenyl-1,2-dihydroquinoline-4-carbonitrile.[1] It may be used in the preparation of highly fluorescent compound, 3-amino-6-methoxy-4-p-tolylsulfonylquinolone.[2]

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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)
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)
Xiaoxiang Zhang et al.
The Journal of organic chemistry, 75(18), 6290-6293 (2010-08-28)
A general and efficient method to prepare 2,4-di- and trisubstituted thiazoles via p-TsOH·H(2)O-catalyzed cyclization of trisubstituted propargylic alcohols with thioamides is described. The reaction was accomplished in moderate to excellent product yields under mild conditions that did not require the
K Eulitz et al.
Lipids, 34(8), 873-877 (1999-10-21)
Conjugated linoleic acid (CLA) mixtures were isomerized with p-toluenesulfinic acid or I2 catalyst. The resultant mixtures of the eight cis/trans geometric isomers of 8,10-, 9,11-, 10,12-, and 11,13-octadecadienoic (18:2) acid methyl esters were separated by silver ion-high-performance liquid chromatography (Ag+-HPLC)
C Bernofsky et al.
Free radical research communications, 9(3-6), 303-315 (1990-01-01)
Adenosine and its nucleotides react with hypochlorite to form unstable products that have been identified as the N6 chloramine derivatives. These chloramines spontaneously oligomerize, form stable adducts with proteins and nucleic acids, and are converted with loss of chlorine to

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