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(5E)-3-(3-chlorophenyl)-2-thioxo-5-[3-(trifluoromethyl)benzylidene]-1,3-thiazolidin-4-one is a complex organic compound characterized by a 1,3-thiazolidin-4-one core structure. It features a 5-[3-(trifluoromethyl)benzylidene] group, which is a benzylidene moiety with a trifluoromethyl group attached to the 3rd carbon of the benzene ring. Additionally, it has a 3-chlorophenyl group attached to the 3rd position of the thiazolidinone ring. The compound is in the E configuration, indicating the geometric arrangement of the double bond. This chemical is known for its potential applications in pharmaceuticals and as a chemical intermediate, particularly in the synthesis of various biologically active compounds.

5726-05-6

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5726-05-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5726-05-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,2 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5726-05:
(6*5)+(5*7)+(4*2)+(3*6)+(2*0)+(1*5)=96
96 % 10 = 6
So 5726-05-6 is a valid CAS Registry Number.

5726-05-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (5E)-3-(3-chlorophenyl)-2-sulfanylidene-5-[[3-(trifluoromethyl)phenyl]methylidene]-1,3-thiazolidin-4-one

1.2 Other means of identification

Product number -
Other names -

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

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More Details:5726-05-6 SDS

5726-05-6Downstream Products

5726-05-6Relevant academic research and scientific papers

An unprecedentedly simple method of synthesis of aryl azides and 3-hydroxytriazenes

Gribanov, Pavel S.,Topchiy, Maxim A.,Golenko, Yulia D.,Lichtenstein, Yana I.,Eshtukov, Artur V.,Terekhov, Vladimir E.,Asachenko, Andrey F.,Nechaev, Mikhail S.

, p. 5984 - 5988 (2018/06/06)

Fischer's approach towards the synthesis of aryl azides and triazinoles from diazonium salts and hydroxylammonium chloride (phenylhydraxylamine) was reinvestigated and optimized. The new methodology enables the preparation of aryl azides and triazinoles in high yields in water at room temperature. The procedure is very simple, robust, easily scalable, reproducible, and "green".

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