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Ethanone, 1-[2-(methylsulfinyl)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

26524-93-6

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26524-93-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26524-93-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,5,2 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 26524-93:
(7*2)+(6*6)+(5*5)+(4*2)+(3*4)+(2*9)+(1*3)=116
116 % 10 = 6
So 26524-93-6 is a valid CAS Registry Number.

26524-93-6Downstream Products

26524-93-6Relevant academic research and scientific papers

Selective oxidations of sulfides to sulfoxides using immobilised cerium alkyl phosphonate

Al-Hashimi, Mohammed,Roy, Gopa,Sullivan, Alice C.,Wilson, John R. H.

, p. 4365 - 4368 (2007/10/03)

A range of sulfides can be selectively oxidised to the corresponding sulfoxides in good yields using catalytic quantities of immobilised cerium alkyl phosphonate and either sodium bromate or tert-butyl hydroperoxide as oxidants.

NEIGHBOURING-GROUP PARTICIPATION IN THE OXIDATION OF SULPHIDES WITH HYDROGEN PEROXIDE

Ruff, Ferenc,Kucsman, Arpad

, p. 241 - 246 (2007/10/02)

Using a set of sulphides (o- and p-XC6H4SMe), the electronic effect, steric hindrance and anchimeric assistance for the O-transfer by H2O2 have been investigated by a kinetic method.The steric effect and anchimeric assistance were evaluated by comparing t

Electronic effect, steric hindrance, and anchimeric assistance in oxidation of sulphides. Neighbouring-group participation through Sulphur-oxygen nonbonded interaction

Ruff, Ferenc,Kucsman, Arpad

, p. 1123 - 1128 (2007/10/02)

Using a set of sulphides o- and p-XC6H4SMe, the electronic effect, steric hindrance, and anchimeric assistance for electrophilic Cl+ addition by TsNHCI and O-transfer by NalO4 were investigated by a kinetic method. The steric effect and anchimeric assistance of the ortho-substituents were evaluated by comparing the reactivity of ortho- and para-substituted compounds (K = ko/kp). For neighbouringgroup activity the following order was obtained: CH2OH ~ CH2OMe ~ CH2CO2Me CH2CO2H ~ CH2NMe2 CH2C02 - ~ CHO CO2Me ~ CO2H COMe ~ CONH2 C02- Reaction rates show that the anchimeric assistance is governed by an S mellip; 0 or S ... N close contact developed in the transition state between oppositely polarized heteroatoms. Factors controlling neighbouringgroup participation through attractive non-bonded interactions are discussed.

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