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5-(methylthio)-4-phenyl-2H-1,2,4-triazol-3(4H)-one is a chemical compound belonging to the class of 1,2,4-triazoles, which are heterocyclic compounds with a five-membered ring containing three nitrogen atoms and one carbon atom. This specific compound features a methylthio group (-SCH3) at the 5-position, a phenyl group (C6H5) at the 4-position, and a ketone group (C=O) at the 3-position. It is an organic molecule with potential applications in pharmaceuticals, agrochemicals, and materials science due to its unique structure and reactivity. The compound's properties, such as solubility, stability, and potential biological activity, can be influenced by the presence of these functional groups, making it a subject of interest for further research and development in various fields.

7746-66-9

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7746-66-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7746-66-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,4 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7746-66:
(6*7)+(5*7)+(4*4)+(3*6)+(2*6)+(1*6)=129
129 % 10 = 9
So 7746-66-9 is a valid CAS Registry Number.

7746-66-9SDS

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 3-methylsulfanyl-4-phenyl-1H-1,2,4-triazol-5-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:7746-66-9 SDS

7746-66-9Relevant academic research and scientific papers

Preparation method of 3-thio-1, 2, 4-triazole compound

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Paragraph 0138; 0139; 0141, (2019/10/02)

The invention provides a preparation method of a 3-thio-1, 2, 4-triazole compound shown as formula I. The method includes the step of: reacting a compound shown as formula II with a compound shown asformula III to obtain the compound shown as formula I in

Synthesis and evaluation of the anticonvulsant activity of 5-alkylthio-4-phenyl-2,4-dihydro-3H-1,2,4-triazol-3-one derivatives

Zheng, Yan,Deng, Xian-Qing,Shu, Bing,Wang, Shi-Ben,Cao, Xu,Quan, Zhe-Shan

, p. 543 - 549 (2013/07/26)

A new series of 5-alkylthio-4-phenyl-2,4-dihydro-3H-1,2,4-triazol-3-one derivatives (4a-w) have been synthesized and tested for their anticonvulsant activity using the maximal electroshock (MES) test. The results indicated that all of the target compounds

N-AMINO ESTERS (BMMA): NOVEL REAGENTS FOR ANNELATION OF PYRIMIDINE MOIETIES

Sauter, Fritz,Froehlich, Johannes,Blasl, Karin,Gewald, Karl

, p. 851 - 866 (2007/10/02)

New reagents for heterocyclic annelations containing a N-amino moiety (=BMMA) were developed and studied regarding their scope and limitations: one-pot reaction with (hetero)aromatic ortho-aminocarbonyl-type model compounds ("car

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