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Benzene, 1,2,4-tris(phenylthio)-, also known as 1,2,4-triphenylbenzene-3-thiol or 1,2,4-triphenylbenzenethiol, is an organic compound with the chemical formula C24H18S3. It is a derivative of benzene, where three phenyl groups are attached to the 1, 2, and 4 positions, and a thiol (-SH) group is present at the 3 position. Benzene, 1,2,4-tris(phenylthio)- is characterized by its aromatic structure and the presence of sulfur atoms, which contribute to its unique chemical properties. It is used in various applications, such as in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. Due to its complex structure and potential reactivity, it is important to handle this chemical with care and follow proper safety protocols.

3379-34-8

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3379-34-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3379-34-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,7 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3379-34:
(6*3)+(5*3)+(4*7)+(3*9)+(2*3)+(1*4)=98
98 % 10 = 8
So 3379-34-8 is a valid CAS Registry Number.

3379-34-8SDS

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 1,2,4-tris(phenylthio)benzene

1.2 Other means of identification

Product number -
Other names 1,2,4-Tris-phenylmercapto-benzol

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:3379-34-8 SDS

3379-34-8Relevant academic research and scientific papers

A semiconducting supramolecular Co(ii)-metallohydrogel: an efficient catalyst for single-pot aryl-S bond formation at room temperature

Dhibar, Subhendu,Dey, Amiya,Jana, Rajkumar,Chatterjee, Arpita,Das, Gourab Kanti,Ray, Partha Pratim,Dey, Biswajit

supporting information, p. 17388 - 17394 (2019/12/02)

A novel mechanically stable supramolecular Co(ii)-metallohydrogel has been synthesized. Cobalt(ii) nitrate hexahydrate and monoethanolamine, as a low molecular weight organic gelator, are used to get the gel. The mechanical stability of the supramolecular hydrogel was analyzed. The morphology of the supramolecular metallohydrogel was scrutinized. The semiconducting features of the metallohydrogel were studied. The conducting properties of the Co(ii)-metallohydrogel establish a Schottky barrier diode type nature. The catalytic nature of the Co(ii)-metallohydrogel based room temperature single pot aryl-S coupling reaction was explored. Most interestingly, the Co(ii)-metallohydrogel based catalytic aryl-S coupling reaction does not require any column-chromatographic purification protocol to get pure aryl-thioethers. Thus, through this work a semiconducting Schottky barrier diode application and catalytic role in the room temperature single pot aryl-S coupling reaction of a supramolecular Co(ii)-metallohydrogel have been explored.

Substitution of Unactivated Aryl Halides by Thiolate Anions in Polyglymes

Pastor, Stephen D.,Hessell, Edward T.

, p. 4812 - 4815 (2007/10/02)

Tetraglyme was found to be a suitable reaction medium to effect the substitution of hexa-, tetra-, tri-, di-, and monochlorobenzenes with sodium alkanethiolates.The substitution of hexa-, tetra-, and trichlorobenzenes by sodium benzenethiolate gave the co

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