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Methanone, (1,4-dioxido-3-phenyl-2-quinoxalinyl)phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13494-38-7

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13494-38-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13494-38-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,9 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13494-38:
(7*1)+(6*3)+(5*4)+(4*9)+(3*4)+(2*3)+(1*8)=107
107 % 10 = 7
So 13494-38-7 is a valid CAS Registry Number.

13494-38-7SDS

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-oxido-4-oxo-3-phenylquinoxalin-4-ium-2-yl)-phenylmethanone

1.2 Other means of identification

Product number -
Other names (1,4-dioxy-3-phenyl-quinoxalin-2-yl)-phenyl-methanone

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:13494-38-7 SDS

13494-38-7Downstream Products

13494-38-7Relevant academic research and scientific papers

Silica gel catalyzed synthesis of quinoxialine 1,4-dioxides under solvent-free conditions using microwave irradiation

Sumiyoshi, Yusuke,Saito, Hiroaki,Miyairi, Shinichi,Takabatake, Tohru

scheme or table, p. 905 - 909 (2009/09/29)

We report on the simple and quick synthesis of quinoxaline 1,4-dioxides in solvent-free conditions under microwave irradiation. Heating of various benzofuroxans and β-ketoesters or 1,3-diketones adsorbed on silica gel in a microwave oven for two minutes affords diverse biologically attractive quinoxaline 1,4-dioxides in high to excellent yields. Silica gel functions not only as support using microwave but also as catalyst and dehydration reagent.

Thermochemical and Theoretical Study of Some Quinoxaline 1,4-Dioxides and of Pyrazine 1,4-Dioxide

Acree Jr.,Powell, Joyce R.,Tucker, Sheryl A.,Ribeiro da Silva, Maria D.M.C.,Matos, M. Agostinha R.,Goncalves,Santos,Morais,Pilcher

, p. 3722 - 3726 (2007/10/03)

The following standard molar enthalpies of formation in the gaseous state at 298.15 K were determined from the enthalpies of combustion of the crystalline solids, and their enthalpies of sublimation and the mean (N-O) bond dissociation enthalpies were derived. ΔfHm0(g); 〈D(N-O)〉 (kJ mol-1): quinoxaline 1,4-dioxide, 227.1 ± 2.4; 255.8 ± 2.0; 2-methylquinoxaline 1,4-dioxide, 169.9 ± 7.2; 268.3 ± 4.9; 2-methyl-3-acetylquinoxaline 1,4-dioxide, 33.1 ± 5.0; 251.6 ± 4.2; 2-phenyl-3-benzoylquinoxaline 1,4-dioxide, 355.2 ± 7.1; 227.3 ± 5.4; 2-methyl-3-carbomethoxyquinoxaline 1,4-dioxide, -148.7 ± 3.2; 242.3 ± 3.9; pyrazine 1,4-dioxide, 186.5 ± 1.9; 254.0 ± 2.3; 2-methyl-5-pyrazinecarboxylic acid, -213.6 ± 1.7. Unconstrained geometry optimizations by ab initio calculations showed the effect of steric hindrance on changes in extended delocalizations and were in accord with the trends in the mean bond dissociation enthalpies.

The reactions of benzofuroxan with carbonyl compounds on the surface of solid catalysts

Takabatake,Hasegawa,Hasegawa

, p. 1477 - 1480 (2007/10/02)

The cyclocondensations of benzofuroxan 1a with carbonyl compounds were smoothly and efficiently carried out by the adsorption of the components on the surface of silica gel or a molecular sieve to form a 2,3-disubstituted quinoxaline 1,4-dioxide. When the

Reactions of Benzofuroxan with 1,3-Diketones or β-Ketoesters on Silica Gel or Alumina

Hasegawa, Minoru,Takabatake, Tohru

, p. 938 (2007/10/02)

The cyclocondensation of benzofuroxan with 1,3-diketones, 3-oxoalkanoic esters, butanedioic esters, or 3-oxoalkanamides in the presence of silica gel (adsorption of the components on silica gel) represents a convenient method for the synthesis of 2,3-disu

Quinoxaline derivatives

-

, (2008/06/13)

The synthesis of quinoxaline and benzimidazole-N-oxides and of ester and amide derivatives of 3-hydroxy-2-quinoxalinecarboxylic acid by a novel process consisting of the reaction between a benzofuroxan and an activated methylene-containing compound under basic conditions.

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