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Benzene, 1-methyl-4-[[[(4-methylphenyl)sulfinyl]methyl]thio]-, (R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38348-10-6

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38348-10-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38348-10-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,3,4 and 8 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 38348-10:
(7*3)+(6*8)+(5*3)+(4*4)+(3*8)+(2*1)+(1*0)=126
126 % 10 = 6
So 38348-10-6 is a valid CAS Registry Number.

38348-10-6Downstream Products

38348-10-6Relevant academic research and scientific papers

A TWO-PHASE REACTION CATALYZED BY A PROTEIN - ASYMETRIC OXIDATION OF FORMALDEHYDE DITHIOACETALS WITH AQUEOUS SODIUM METAPERIODATE

Ogura, Katsuyuki,Fujita, Makoto,Iida, Hirotada

, p. 2233 - 2236 (1980)

We examined whether a protein could catalyze two-phase oxidation of formaldehyde dithioacetals with aqueous sodium metaperiodate and bovine serum albumin was found to be effective and give the corresponding S-oxides in optically active forms.

AN IMPROVED PROCEDURE FOR EFFICIENT GENERATION OF METHYL(OR p-TOLYL)THIOMETHYL GRIGNARD REAGENT AND ITS USE IN ORGANIC SYNTHESES

Ogura, Katsuyuki,Fujita, Makoto,Takahashi, Kazumasa,Iida, Hirotada

, p. 1697 - 1698 (2007/10/02)

The optimal condition for transformation of a chloromethyl sulfide into the corresponding Grignard reagent (2) in a high yield are established and 2 is shown to react with various functional groups such as an alkyl halide, an aldehyde, and a sulfinic este

Stereoselective Enzyme-catalysed Oxidation-Reduction Reactions of Thioacetals-Thioacetal Sulphoxides by Fungy

Auret, Barbara J.,Boyd, Derek R.,Breen, Fiona,Greene, Ruth M. E.,Robinson, Peter M.

, p. 930 - 933 (2007/10/02)

Enzymes present in the fungus Mortierella isabellina catalyse the transfer of an oxygen atom to the cyclic thioacetal 1,3-dithian and from 1,3-dithian 1-oxide, 1,3,5-trithian 1-oxide, and cis-1,3-dithian 1,3-dioxide.The oxidation of 1,3-dithian and the acyclic thioacetal bis-(p-tolylthio)methane to form the corresponding monosulphoxides occurred in the presence of growing cultures of Aspergillus foetidus and a Helminthosporium species.The degree and the preferred direction of stereoselectivity occurring during the asymmetric oxidation and reduction steps was deduced from the enantiomeric excess (e.e.) and absolute stereochemistry of the isolated 1,3-dithian 1-oxide and p-tolylthio-(p-tolylsulphinyl)metane.

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