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13133-62-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13133-62-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,3 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 13133-62:
65 % 10 = 5
So 13133-62-5 is a valid CAS Registry Number.



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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017


1.1 GHS Product identifier

Product name thiophenolate

1.2 Other means of identification

Product number -
Other names thiophenoxide ion

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:13133-62-5 SDS

13133-62-5Relevant articles and documents


DePuy, Charles H.,Bierbaum, Veronica M.

, p. 5129 - 5130 (1981)

Many gas-phase anions react with carbonyl sulfide by sulfur atom transfer to form RS(1-) ions.The properties of H2NS(1-), formed in this way from H2N(1-) and OCS, are described.

Mesolysis Mechanisms of Aromatic Thioether Radical Anions Studied by Pulse Radiolysis and DFT Calculations

Yamaji, Minoru,Tojo, Sachiko,Fujitsuka, Mamoru,Sugimoto, Akira,Majima, Tetsuro

, p. 7890 - 7895 (2015/09/01)

The mesolysis mechanisms for eight aromatic thioether radical anions (ArCH2SAr′?-) generated during radiolysis in 2-methyltetrahydrofuran were studied by spectroscopic measurements and DFT calculation. Seven of ArCH2SAr′s

Generation of alkoxycarbenium ion pools from thioacetals and applications to glycosylation chemistry

Suzuki, Shinkiti,Matsumoto, Kouichi,Kawamura, Kohsuke,Suga, Seiji,Yoshida, Jun-Ichi

, p. 3755 - 3758 (2007/10/03)

(Chemical Equation Presented) Alkoxycarbenium ions have been generated and accumulated as "cation pools" by the low-temperature electrochemical oxidation of α-phenylthioethers. Although an unsuccessful attempt to accumulate glycosyl cations was made, a one-pot method for electrochemical glycosylation, which involves anodic oxidation of thioglycosides to generate glycosyl cation equivalents followed by their reactions with glycosyl acceptors, has been developed.

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