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934-72-5

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934-72-5 Usage

Uses

Methyl p-tolyl sulfoxide may be used as a catalyst in the preparation of homoallylic alcohols by the allylation of aldehydes with allyltrichlorosilane. It may be used as a ligand in the synthesis of molybdenum chlorocomplexes.

Synthesis Reference(s)

Chemistry Letters, 15, p. 967, 1986Synthetic Communications, 19, p. 1569, 1989 DOI: 10.1080/00397918908051052Tetrahedron Letters, 19, p. 3415, 1978

General Description

Methyl p-tolyl sulfoxide (MTSO), an alkyl-substituted p-tolyl sulfoxide, is a Lewis base. It behaves as an activator of silicon tetrachloride that is employed in aza-Diels-Alder reaction.

Check Digit Verification of cas no

The CAS Registry Mumber 934-72-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,3 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 934-72:
(5*9)+(4*3)+(3*4)+(2*7)+(1*2)=85
85 % 10 = 5
So 934-72-5 is a valid CAS Registry Number.
InChI:InChI=1S/C8H10OS/c1-7-3-5-8(6-4-7)10(2)9/h3-6H,1-2H3

934-72-5 Well-known Company Product Price

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  • Aldrich

  • (481858)  Methylp-tolylsulfoxide  97%

  • 934-72-5

  • 481858-5G

  • 1,535.04CNY

  • Detail

934-72-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl p-tolyl sulfoxide

1.2 Other means of identification

Product number -
Other names 1-methyl-4-methylsulfinylbenzene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:934-72-5 SDS

934-72-5Relevant articles and documents

Unexpected nucleophilic participation and rearrangement of DBU in reactions with saccharin derivatives

Bulman Page, Philip C.,Vahedi, Hooshang,Bethell, Donald,Barkley, James V.

, p. 1937 - 1941 (2003)

DBU attacks saccharin derivatives with subsequent rearrangement to give rise to 3-[3′-(1″-azepin-2″-onyl)propylamino]-1, 2-benzisothiazole-1,1-dioxide 2 after work-up.

Niobium(V) oxido tris-carbamate as easily available and robust catalytic precursor for the selective sulfide to sulfone oxidation

Bresciani, Giulio,Ciancaleoni, Gianluca,Crucianelli, Marcello,Gemmiti, Mario,Marchetti, Fabio,Pampaloni, Guido

, (2021/11/01)

The oxidation of the sulfide function promoted by a variety of vanadium compounds has been largely explored, whereas the use of homogeneous catalytic systems based on the heavier group 5 metals remains less explored. We report the use of easily available niobium and tantalum carbamates, i.e. [M(O2CNMe2)5] (M = Nb, 1; M = Ta, 2), [Nb(O2CNMe2)4], 3, [NbO(O2CNEt2)3], 4, and [NbCl3(O2CNEt2)2], 5, as effective catalysts for the conversion of a series of alkyl aryl and aromatic sulfides into the corresponding sulfones. NMR investigations on the performant niobium catalyst 4 unexpectedly revealed the substantial stability of this compound in the protic catalytic environment, and a plausible catalytic cycle was obtained by DFT studies. The two active catalytic species, i.e. 4 and its minor mono-methoxide derivative, presumably interconvert to each other exploiting the versatile coordination of the carbamato ligand.

Air atmospheric photocatalytic oxidation by ultrathin C,N-TiO2nanosheets

Cheng, Xiuyan,Zhang, Jianling,Liu, Lifei,Zheng, Lirong,Zhang, Fanyu,Duan, Ran,Sha, Yufei,Su, Zhuizhui,Xie, Fei

supporting information, p. 1165 - 1170 (2021/02/26)

Herein, we demonstrate the highly efficient photocatalytic sulfide oxidation reaction under mild conditions,i.e.in air, at room temperature and in the absence of a sacrificial reagent, co-catalyst or redox mediator, by using ultrathin C,N-TiO2nanosheets as a photocatalyst.

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