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3H-1,2,4-Triazol-3-one, 2,4-dihydro-5-(4-methoxyphenyl)-2,4-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

104707-62-2

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104707-62-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104707-62-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,7,0 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 104707-62:
(8*1)+(7*0)+(6*4)+(5*7)+(4*0)+(3*7)+(2*6)+(1*2)=102
102 % 10 = 2
So 104707-62-2 is a valid CAS Registry Number.

104707-62-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(4-methoxyphenyl)-4-phenyl-2-phenyl-2H-1,2,4-triazol-3(4H)-one

1.2 Other means of identification

Product number -
Other names 5-(4-Methoxy-phenyl)-2,4-diphenyl-2,4-dihydro-[1,2,4]triazol-3-one

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:104707-62-2 SDS

104707-62-2Downstream Products

104707-62-2Relevant academic research and scientific papers

Synthesis of 1,2,4-Triazol-3-imines via Selective Stepwise Cycloaddition of Nitrile Imines with Organo-cyanamides

Sharma, Pallavi,Bhat, Shreesha V.,Prabhath, M. R. Ranga,Molino, Andrew,Nauha, Elisa,Wilson, David J. D.,Moses, John E.

, p. 4263 - 4266 (2018/07/29)

A convenient method for the synthesis of 1,2,4-triazol-3-imines through a selective, formal, 1,3-dipolar cycloaddition of organo-cyanamide ions with nitrile imine dipoles is reported. Hydrolysis of the 1,2,4-triazol-3-imines yields the corresponding 1,2,4-triazol-5-ones. A stepwise mechanism, supported by DFT calculations, is invoked to explain the reaction selectivity.

Microwave assisted one-pot tandem three-component synthesis of 2,4,5-triary1-2-4-dihydro-3H-1,2,4-triazol-3-one derivatives

Mohammadi, Bagher,Adib, Mehdi

, p. 553 - 556 (2014/05/06)

This work described a one-pot tandem three-component synthesis of 2,4,5-triaryl-2,4-dihydro-3H-1,2,4-triazol-3-ones using a simple reaction between phenylhydrazines, benzaldehydes and phenyl isocyanates under microwave irradiation and solvent-free conditi

Reactions of Sulfur Monochloride with some Aromatic Aldehyde Semicarbazones and Thiosemicarbazones: New Syntheses of Substituted 2,4-Dihydro-1,2,4-triazol-3-ones, 2,4-Dihydro-1,2,4-triazole-3-thiones and 2-Amino-1,3,4-oxadiazoles

Milcent, Rene,Nguyen, Thu-Huong

, p. 881 - 883 (2007/10/02)

Treatment of various substituted semicarbazones of aromatic aldehydes with sulfur monochloride yields the corresponding substituted 2,4-dihydro-1,2,4-triazol-3-ones.With thiosemicarbazones, the products are derivatives either of the 2-amino-1,3,4-thiadiaz

Oxidation of Aldehyde Semicarbazones with Lead Dioxide: Application to the Syntheses of 2-Amino-1,3,4-oxadiazoles and 2,4-Dihydro-1,2,4-triazol-3-ones

Nguyen, Thu-Huong,Milcent, Rene,Barbier, Geo

, p. 1383 - 1388 (2007/10/02)

The oxidation of aldehyde semicarbazones with lead dioxide in acid media was effected.The 4,4-disubstituted semicarbazones of aromatic aldehydes afford 2-amino-1,3,4-oxadiazole derivatives.The 2,4-disubstituted semicarbazones give 2,4-dihydro-1,2,4-triazo

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