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5-benzylidene-3-phenyl-1,3-thiazolidine-2,4-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

42518-27-4

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42518-27-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42518-27-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,5,1 and 8 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 42518-27:
(7*4)+(6*2)+(5*5)+(4*1)+(3*8)+(2*2)+(1*7)=104
104 % 10 = 4
So 42518-27-4 is a valid CAS Registry Number.

42518-27-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-benzylidene-3-phenyl-1,3-thiazolidine-2,4-dione

1.2 Other means of identification

Product number -
Other names 5-benzylidene-3-phenyl-imidazolidine-2,4-dione

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:42518-27-4 SDS

42518-27-4Relevant academic research and scientific papers

Ionic liquid-accelerated N-arylation of 5-arylidene-2,4-thiazolidinediones with diaryliodonium salts

Yang, De-Hong,Gao, Hong-Liang,Yang, Ben-Yong,Chen, Zhen-Chu

experimental part, p. 686 - 687 (2009/09/06)

An efficient method for the synthesis of N-aryl-5-arylidene-2,4- thiazolidinediones has been developed involving the N-arylation of 5-arylidene-2,4-thiazolidinediones derivatives with diaryliodonium salts in the ionic liquid [bmim]PF6 (1-butyl-

Introduction of Selenium to Heterocyclic Compounds. Part VII. Synthesis of 3-Alkyl-5-benzylidene- and 3-Alkyl-5-cinnamylidene-2-selenorhodanines

Tejchman, W.,Korohoda, M. J.

, p. 1315 - 1322 (2007/10/03)

Five new 3-alkyl-5-benzylidene- and five new 3-alkyl-5-cinnamylidene-2-selenorhodanines were obtained by treatment of methylation products of appropriate rhodanines with H2Se. The stability of 2-thiazolinium salts with SCH3 or RNHCH3 group formed during methylation (cf. Scheme 2) is determined by substituents at C-5 and N-3 atoms.

Introduction of selenium to heterocyclic compounds. Part VI. Synthesis of 3-aryl-5-benzylidene- and 3-aryl-5-cinnamylidene-2-selenorhodanines

Tejchman,Korohoda

, p. 1124 - 1134 (2007/10/03)

Three new 3-aryl-5-benzylidene-2-selenorhodanines and seven new 3-aryl-5-cinnamylidene-2-selenorhodanines were obtained by treatment with H2Se of methylation products of appropriate 2-iminothiazolidine-4-one derivatives.

Oxidations of Thiourethanes, 10.- Synthesis, Crystal Structures, Oxidation and Photochemistry of Thione S-Oxides of Cyclic Dithiourethanes and Dithiocarbazates

Hanefeld, Wolfgang,Schlitzer, Martin,Schuetz, Harald,Wocadlo, Sigrid,Massa, Werner

, p. 337 - 344 (2007/10/02)

Several cyclic dithiocarbamates and dithiocarbazates (2-4) have been oxidised with mCPBA to give the correspnding thione S-oxides 5-7.The sulfine structure was confirmed by oxidation to the corresponding oxo derivatives and X-ray crystal structures analys

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