Ethylen-S,S'-4-toluolthiosulfonat Chemische Eigenschaften,Einsatz,Produktion Methoden

S-S?tze Betriebsanweisung:

S22:Staub nicht einatmen.
S24/25:Berührung mit den Augen und der Haut vermeiden.

Synthese

Treatment of potassium thiotosylate, itself made by the reaction of p-Toluenesulfonyl Chloride with Potassium Hydrogen Sulfide, with 1,3-dibromopropane or 1,2-dibromoethane in the presence of Potassium Iodide affords 1,3-propanedithiol bis(p-toluenesulfonate) and 1,2-ethanedithiol bis(p-toluenesulfonate), respectively.

Ethylen-S,S'-4-toluolthiosulfonat Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte

Ethylen-S,S'-4-toluolthiosulfonat Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Firmenname	Telefon	E-Mail	Land	Produktkatalog	Edge Rate
Aladdin Scientific		tp@aladdinsci.com	United States	52923	58
J & K SCIENTIFIC LTD.	18210857532; 18210857532	jkinfo@jkchemical.com	China	96815	76
Meryer (Shanghai) Chemical Technology Co., Ltd.	4006356688 18621169109	market03@meryer.com	China	40228	62
Beijing Donghualituo Techonlogy Development Co.,Ltd.	010-88425576	sales@dhltchem.com	China	793	59
TCI (Shanghai) Development Co., Ltd.	021-67121386	Sales-CN@TCIchemicals.com	China	24529	81
Energy Chemical	021-021-58432009 400-005-6266	sales8178@energy-chemical.com	China	44816	61
Hunan Hui Bai Shi Biotechnology Co., Ltd.	0731-85526065 13308475853	ivy@hnhbsj.com	China	7237	62
Hangzhou Yuhao Chemical Technology Co., Ltd	--	info@yuhaochemical.com	China	6387	52
TOKYO CHEMICAL INDUSTRY CO., LTD.	03-36680489	Sales-JP@TCIchemicals.com	Japan	28387	80
TCI Europe	320-37350700	sales@tcieurope.eu	Europe	23671	75

2225-23-2(Ethylen-S,S'-4-toluolthiosulfonat)Verwandte Suche:

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• 1,1'-[Ethylenebisthiobissulfonyl]bis(4-methylbenzene)
• Ethylenebis(tosyl sulfide)
• p-Toluenesulfonothioic acid S-[2-[(4-methylphenyl)sulfonylthio]ethyl] ester
• 1,2-Di(p-tosylthio)ethane 1,2-Ethanedithiol Ditosylate Ethylene Bis(p-toluenethiosulfonate) S,S'-Ethylene p-Toluenethiosulfonate
• 1-methyl-4-[2-(4-methylphenyl)sulfonylsulfanylethylsulfanylsulfonyl]benzene
• 1-methyl-4-[2-[(4-methylphenyl)sulfonylthio]ethylthio]sulfonyl-benzene
• 1,2-ETHANEDITHIOL DITOSYLATE
• 1,2-DI(P-TOSYLTHIO)ETHANE
• ETHYLENE DI(THIOTOSYLATE)
• ETHYLENE BIS(P-TOLUENETHIOSULFONATE)
• ethylene S,S'-4-toluenethiosulphonate
• S,S'-ETHYLENE DI(P-TOLUENETHIOSULFONATE)
• S S'-ETHYLENE P-TOLUENETHIOSULFONATE 9&
• protectingreagentforactivemethylene
• Ethylene Di(thiotosylate) [Protecting Reagent for Active Methylene]
• S,S'-ETHYLENE P-TOLUENETHIOSULFONATE
• 1,2-Di(p-tosylthio)ethane, 1,2-Ethanedithiol ditosylate, Ethylene di(thiotosylate)
• 1,1'-[Ethylenebis[thio(sulfonyl)]]bis(4-methylbenzene)
• EthyleneDi(thiotosylate)[ProtectingReagentforActiveMethylene]>
• Benzenesulfonothioic acid, 4-methyl-, S1,S1'-1,2-ethanediyl ester
• S,S'-(ethane-1,2-diyl) bis(4-methylbenzenesulfonothioate)
• Ethylene di
• 2225-23-2
• C16H18O4S4
• CH3C6H4SO2SCH2CH2SSO2C6H4CH3
• Sulfur Compounds (for Synthesis)
• Protection & Derivatization Reagents (for Synthesis)
• Protection & Derivatization Reagents (for Synthesis)
• Sulfur Compounds (for Synthesis)
• Synthetic Organic Chemistry