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4-(benzylsulfinyl)butan-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88738-53-8

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88738-53-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88738-53-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,7,3 and 8 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 88738-53:
(7*8)+(6*8)+(5*7)+(4*3)+(3*8)+(2*5)+(1*3)=188
188 % 10 = 8
So 88738-53-8 is a valid CAS Registry Number.

88738-53-8Downstream Products

88738-53-8Relevant academic research and scientific papers

Pt(II) coordination complexes as visible light photocatalysts for the oxidation of sulfides using batch and flow processes

Casado-Sánchez, Antonio,Gómez-Ballesteros, Rocío,Tato, Francisco,Soriano, Francisco J.,Pascual-Coca, Gustavo,Cabrera, Silvia,Alemán, José

supporting information, p. 9137 - 9140 (2016/07/21)

A new catalytic system for the photooxidation of sulfides based on Pt(ii) complexes is presented. The catalyst is capable of oxidizing a large number of sulfides containing aryl, alkyl, allyl, benzyl, as well as more complex structures such as heterocycles and methionine amino acid, with complete chemoselectivity. In addition, the first sulfur oxidation in a continuous flow process has been developed.

GOLD(III) CATALYZED OXIDATION OF SULFIDES TO SULFOXIDES BY NITRIC ACID UNDER PHASE-TRANSFER CONDITIONS: A NEW SYNTHESIS OF SULFOXIDES

Gasparrini, F.,Giovannoli, M.,Misiti, D.,Natile, G.,Palmieri, G.

, p. 3181 - 3184 (2007/10/02)

Gold(III) halides catalyze the oxidation of sulfides to sulfoxides in a phase-transfer process.The organic sulfides, dissolved in nitromethane, are treated with (Bu4N(1+)*AuCl4(1-)) in catalytic amount and aqueous nitric acid wich acts as an oxidant.The oxidation of the thio-group is selective and can be carried out also in the presence of other oxidizable groups, such as vinyl, tertiary amino, hydroxy, diol etc, which are left unchanged.Moreover in the case of asymmetric disulfides the reaction is regiospecific leading to the fomation of a single monosulfoxide.

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