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Triphenylsulfonium hydroxide, also known as triphenylsulfonium hydrate or triphenylsulfonium hydroxide salt, is a chemical compound with the formula (C6H5)3S+OH-. It is a colorless, crystalline solid that is soluble in water and polar organic solvents. Triphenylsulfonium hydroxide is widely used as a phase-transfer catalyst in organic synthesis, particularly in the preparation of various organic compounds, such as esters, amides, and nitriles. Triphenylsulfonium hydroxide is also employed in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique properties, such as high reactivity and selectivity, make it a valuable tool in the field of organic chemistry.

58621-56-0

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58621-56-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58621-56-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,6,2 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 58621-56:
(7*5)+(6*8)+(5*6)+(4*2)+(3*1)+(2*5)+(1*6)=140
140 % 10 = 0
So 58621-56-0 is a valid CAS Registry Number.

58621-56-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name triphenylsulfanium,hydroxide

1.2 Other means of identification

Product number -
Other names Triphenylsulfonium hydroxide

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:58621-56-0 SDS

58621-56-0Downstream Products

58621-56-0Relevant academic research and scientific papers

REACTION OF BENZENE WITH DIPHENYL SULFOXIDES

Endo, Yasuyuki,Shudo, Koichi,Okamoto, Toshihiko

, p. 3753 - 3755 (2007/10/02)

Diphenyl sulfoxide reacted with benzenes in the presence of trifluoroacetic anhydride and trifluoromethanesulfonic acid to yield triphenylsulfonium ions in good yields.A new electrophilic spacies was proposed. - Keywords: electrophilic aromatic substituti

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