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6406-91-3

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6406-91-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6406-91-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,0 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6406-91:
(6*6)+(5*4)+(4*0)+(3*6)+(2*9)+(1*1)=93
93 % 10 = 3
So 6406-91-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H8O2S/c1-7-6-12(10,11)9-5-3-2-4-8(7)9/h2-6H,1H3

6406-91-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-1-benzothiophene 1,1-dioxide

1.2 Other means of identification

Product number -
Other names 3-Methylbenzo<b>thiophen-1,1-dioxid

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:6406-91-3 SDS

6406-91-3Relevant articles and documents

-

Aleksanyan et al.

, p. 264,265 (1965)

-

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.

A new phosphotungstate-supported rhenium carbonyl derivative: Synthesis, characterization and catalytic selective oxidation of thiophenes

Lu, Jingkun,Feng, Junwei,Ma, Xinyi,Wang, Ping,Xu, Baijie,He, Peipei,Jia, Jiage,Ma, Pengtao,Niu, Jingyang,Wang, Jingping

, p. 7322 - 7328 (2019/12/09)

A monomeric phosphotungstate-supported rhenium carbonyl derivative, [N(CH3)4]6H4[P2W17O62{Re(CO)3}2]·25H2O (1), has been synthesized in a conventional solution system and structurally characterized by single crystal X-ray diffraction crystallography, IR spectroscopy, thermogravimetric (TG) analyses, X-ray powder diffraction (XRPD), and electrospray ionization mass spectrometry (ESI-MS). To our knowledge, this is the first time that the {Re2} fragment existing in the polyoxoanion has been observed in polyoxometalate-supported metal carbonyl derivatives. Moreover, UV-vis spectroscopy was employed to elucidate the stability of the polyoxoanion, and its electrochemical properties were also investigated. In particular, complex 1 could act as an efficient homogeneous catalyst for selective oxidation of thiophenes. For example, dibenzothiophene (DBT) undergoes up to 99% conversion and 99% sulfone selectivity in acetonitrile with 30% H2O2 as an oxidant.

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