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621-08-9

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621-08-9 Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 60, p. 8365, 1995 DOI: 10.1021/jo00131a009

Flammability and Explosibility

Notclassified

Check Digit Verification of cas no

The CAS Registry Mumber 621-08-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 621-08:
(5*6)+(4*2)+(3*1)+(2*0)+(1*8)=49
49 % 10 = 9
So 621-08-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H14OS/c15-16(11-13-7-3-1-4-8-13)12-14-9-5-2-6-10-14/h1-10H,11-12H2

621-08-9SDS

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 Benzyl sulfoxide

1.2 Other means of identification

Product number -
Other names Benzene, 1,1‘-[sulfinylbis(methylene)]bis-

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:621-08-9 SDS

621-08-9Relevant articles and documents

Haake,Turley

, p. 4611,4614 (1967)

Nicholson

, p. 2539,2543 (1954)

In Situ Generated Organic Peroxides in Oxidative Desulfurization of Naphtha Reformate

Akopyan, A. V.,Anisimov, A. V.,Eseva, E. A.,Sinikova, N. A.

, p. 472 - 482 (2021/06/01)

Abstract: The paper describes a method developed for the oxidation of organosulfur compounds using organic peroxides generated in situ under the action of atmospheric oxygen on gasoline fraction after reforming. Naphtha reformate that contained dibenzothiophene as a model substrate was subjected to oxidative desulfurization by organic peroxides generated in situ under atmospheric oxygen. The study examined various catalytic systems, including immobilized Anderson-type polyoxometalates, and initiators, which, in combination, provided effective generation of alkyl hydroperoxides, selective oxidation of organosulfur compounds in the hydrocarbon feedstock, and a high conversion rate.

Fullerene soot and a fullerene nanodispersion as recyclable heterogeneous off-the-shelf photocatalysts

Jozeliūnait?, Augustina,Val?eckas, Domantas,Orentas, Edvinas

, p. 4104 - 4111 (2021/02/02)

Metal-free heterogeneous photocatalysis, which requires no prior catalyst immobilization or chemical modification and can operate in green solvents, represents a highly-sought after, yet currently still underdeveloped, synthetic method. In this report we present a comparative study which aims to evaluate the use of unmodified fullerene soot and a fullerene nanodispersion as non-soluble and quasi-soluble carbon-based photocatalysts, respectively, for sulfide oxidation and other transformations using oxygen as an oxidant in ethanol. A wide range of sulfoxides were successfully prepared with good yields and chemoselectivity using a very low catalyst loading. The fullerene soot photocatalyst is easily recovered and shows excellent stability of the catalytic properties. The reaction was shown to proceed via a singlet oxygen pathway and has a high selectivity for aliphatic sulfides, whereas the oxidation of thioanisoles can be accomplished using an amine mediated electron transfer mechanism. The applicability of the fullerene nanodispersion as a general purpose photocatalyst was demonstrated in radical cyclization, boronic acid oxidation and imine formation reactions.

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