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2,3-diphenyl-N-(1-phenylethyl)quinoxaline-6-carboxamide is a complex organic compound with the molecular formula C28H22N2O. It is characterized by a quinoxaline ring system, which is a fused bicyclic structure consisting of a pyrazine and a benzene ring. The compound features two phenyl groups attached to the quinoxaline at the 2 and 3 positions, and a phenylethyl group as a substituent on the nitrogen atom. The carboxamide functional group is located at the 6 position of the quinoxaline ring. This chemical is known for its potential applications in pharmaceutical research, particularly as a precursor or intermediate in the synthesis of various biologically active molecules. Its structure and properties make it a candidate for further exploration in drug development, given its ability to form stable complexes and interact with biological targets.

7047-07-6

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7047-07-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7047-07-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,4 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7047-07:
(6*7)+(5*0)+(4*4)+(3*7)+(2*0)+(1*7)=86
86 % 10 = 6
So 7047-07-6 is a valid CAS Registry Number.

7047-07-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-diphenyl-N-(1-phenylethyl)quinoxaline-6-carboxamide

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

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More Details:7047-07-6 SDS

7047-07-6Relevant articles and documents

DESMETHYLANETHOLE TRITHIONE DERIVATIVES FOR THE TREATMENT OF DISEASES LINKED TO MITOCHONDRIAL REACTIVE OXYGEN SPECIES (ROS) PRODUCTION

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Page/Page column 89; 90, (2018/09/28)

The present invention relates to desmethylanethole trithione ( AOX ) and derivatives thereof, especially derivatives of formula (I), for the prevention and treatment of diseases whose initiation and/or evolution relates to the production and effects of re

SULFUR TRANSFER REAGENTS FOR OLIGONUCLEOTIDE SYNTHESIS

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, (2011/06/24)

The use of N-formamidino-5-amino-3H-1,2,4-dithiazole-3-thiones, 5-phenyl-3H-1,2,4-dithiazole-3-thiones, and derivatives thereof as novel, efficient sulfur-transfer reagents is disclosed. Sulfur transfer from these reagents to compounds containing a P(III) atom (e.g., triphenylphosphine, 5′-O-DMT-thymidine 2-cyanoethyl-(N,N-diisopropyl)phosphoramidite, and 5′-O-DMT-3′-O-levulinyl dithymidilyl 2-cyanoethyl phosphite), was studied in solution by 31P NMR and HPLC. The sulfur transfer from title compounds was also studied in the solid-phase synthesis of oligonucleotide phosphorothioates by phosphoramidite methods. In this application, the efficiency of the sulfur transfer reaction for 2′-deoxyoligonucleotides was better than 99.5%. The novel sulfurizing agents are synthesized, at low cost, using simple chemical methods. As opposed to many sulfur transfer reagents known in the prior art such as 1,2-benzodithiol-3-one-1,1-dioxide (Beaucage reagent) and 5-ethoxy-3H-1,2,4-dithiazole-2-one (EDIT), the sulfurizing agents disclosed herein are highly stable in solution, which increases their practical and commercial value.

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