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1-METHYL-4-((3-[(4-METHYLPHENYL)SULFANYL]PROPYL)SULFANYL)BENZENE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25741-56-4

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25741-56-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25741-56-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,7,4 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 25741-56:
(7*2)+(6*5)+(5*7)+(4*4)+(3*1)+(2*5)+(1*6)=114
114 % 10 = 4
So 25741-56-4 is a valid CAS Registry Number.

25741-56-4Relevant academic research and scientific papers

Silica: An efficient catalyst for one-pot regioselective synthesis of dithioethers

Kundu, Samir,Roy, Babli,Basu, Basudeb

, p. 26 - 33 (2014/01/23)

The development of a silica-promoted highly selective synthesis of 1,2 or 1,3-dithioethers via solvent-free one-pot tandem reactions of an allyl bromide with excess thiol at room temperature is described. The choice of silica gel, either pre-calcined or moistened with water, exhibited notable regioselectivity in the formation of dithioethers. Plausible mechanistic routes were explored and postulated.

A synthesis of diketones from carbonyl compounds and α,ω-dichloro-α,ω-disulfinylalkanes with two carbon-carbon bond-formation via bis-sulfinyloxiranes

Satoh, Tsuyoshi,Taguchi, Daisaku,Kurabayashi, Aki,Kanoto, Makiko

, p. 4217 - 4224 (2007/10/03)

Bis-sulfinyloxiranes were synthesized in two steps from carbonyl compounds and α,ω-dichloro-α,ω-disulfinylalkanes, which were synthesized from α,ω-dibromoalkanes in three steps, in good yields. Treatment of the bis-sulfinyloxiranes with sodium benzenethiolate and piperidine gave α,α′-di(phenylthio) diketones and α,α′-diamino diketones, respectively, in high yields. From these products, some kinds of diketones were synthesized in good to high yields.

A New and Convenient Synthetic Method for Cyclopropyl Phenyl Sulfides

Tanaka, Kazuhiko,Uneme, Hideki,Matsui, Shuichi,Kaji, Aritsune

, p. 2965 - 2972 (2007/10/02)

The reactions of a variety of 1,3-bis(phenylthio)propanes with butyllithium have been shown to produce cyclopropyl phenyl sulfides in good to high yields.A new and convenient in situ preparation of 1-lithiocyclopropyl phenyl sulfide can be readily carried out by treating 1,3-bis(phenylthio)propane with 2 equiv. of butyllithium at 0 degC in THF.The reaction with electrophiles proceeds in good yield.O-Aryl and O-alkyl S-cyclopropyl dithiocarbonates also can be prepared in good yields. 1,2-Bis(phenylthio)ethane was converted to phenyl vinyl sulfide on treatment with butyllithium, while 1,4-bis(phenylthio)butane was recovered unchanged by a similar treatment.

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