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592-22-3

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592-22-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 592-22-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,9 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 592-22:
(5*5)+(4*9)+(3*2)+(2*2)+(1*2)=73
73 % 10 = 3
So 592-22-3 is a valid CAS Registry Number.
InChI:InChI=1/C4H6O2S2/c1-2(5)3(6)4(7)8/h4,7-8H,1H3

592-22-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name DIACETYLDITHIOL

1.2 Other means of identification

Product number -
Other names Disulfide, diacetyl

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:592-22-3 SDS

592-22-3Relevant articles and documents

I 2 as a mild and efficient catalyst in deoxygenation of sulfoxides with thioacetic acid

Jabbari, Arida,Zarei, Morteza,Jamaleddini, Azar

, p. 413 - 418 (2012/10/29)

An effective procedure for deoxygenation of sulfoxides to sulfides using thioacetic acid as a reducing agent and a catalytic amount of I2 in MeCN at ambient temperature has been developed. Using this protocol, a variety of sulfoxides including benzyl, allyl, alkyl and aryl sulfoxides have been successfully reduced to the corresponding sulfides in excellent yields.

Synthesis of isothiocyanates by reaction of amides with carbon disulfide in the presence of solid potassium carbonate/sodium hydroxide mixture

Albanese,Penso

, p. 1001 - 1002 (2007/10/02)

Readily available N-monosubstituted trifluoroacetamides are transformed into isothiocyanates in good yield by reaction, at room temperature, with carbon disulfide in acetonitrile in the presence of anhydrous sodium hydroxide/potassium carbonate basic mixture.

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