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1684-14-6

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1684-14-6 Usage

Chemical Properties

light beige or grey solid

Synthesis Reference(s)

Tetrahedron Letters, 17, p. 2347, 1976 DOI: 10.1016/S0040-4039(00)78773-9

Check Digit Verification of cas no

The CAS Registry Mumber 1684-14-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,8 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1684-14:
(6*1)+(5*6)+(4*8)+(3*4)+(2*1)+(1*4)=86
86 % 10 = 6
So 1684-14-6 is a valid CAS Registry Number.
InChI:InChI=1/C20H14N2/c1-3-9-15(10-4-1)19-20(16-11-5-2-6-12-16)22-18-14-8-7-13-17(18)21-19/h1-14H

1684-14-6 Well-known Company Product Price

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  • (Code)Product description
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  • Detail
  • Alfa Aesar

  • (B20100)  2,3-Diphenylquinoxaline, 98+%   

  • 1684-14-6

  • 5g

  • 301.0CNY

  • Detail
  • Alfa Aesar

  • (B20100)  2,3-Diphenylquinoxaline, 98+%   

  • 1684-14-6

  • 25g

  • 932.0CNY

  • Detail
  • Alfa Aesar

  • (B20100)  2,3-Diphenylquinoxaline, 98+%   

  • 1684-14-6

  • 100g

  • 1787.0CNY

  • Detail

1684-14-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-Diphenylquinoxaline

1.2 Other means of identification

Product number -
Other names 2,3-DIPHENYLQUINOXALINE

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:1684-14-6 SDS

1684-14-6Related news

Color tuning of red phosphorescence: New iridium complexes containing fluorinated 2,3-DIPHENYLQUINOXALINE (cas 1684-14-6) ligands09/27/2019

The new iridium complexes containing a derivative of 2,3-diphenylquinoxaline as an emitting ligand were synthesized, and their photophysical properties were investigated. The complexes prepared in this study were bis(6-F-2,3-di(p-fluorophenyl) quinoxalinato)iridium acetylacetonate (Ir(6-F-2,3-dp...detailed

New 2,3-DIPHENYLQUINOXALINE (cas 1684-14-6) containing organic D-A-π-A dyes with nickel oxide photocathode prepared by surfactant-mediated synthesis for high performance p-type dye-sensitized solar cells09/26/2019

Dye-sensitized solar cells (DSSCs) are one of the most promising organic photovoltaics. The optimized efficiency of a tandem cell combined with both n- and p-type DSSCs was theoretically predicted to be 43%. The bottleneck for reaching the optimized performance is limited by the p-type half-cell...detailed

Highly efficient solution-processed pure red phosphorescent organic light-emitting diodes using iridium complexes based on 2,3-DIPHENYLQUINOXALINE (cas 1684-14-6) ligand09/25/2019

We synthesized two highly efficient red phosphorescent Ir(III) complexes, bis[2,3-diphenylquinoxalinato-N,C2′]iridium(III) pyrazinate (dpq)2Ir(prz) (1) and bis[2,3-diphenylquinoxalinato- N,C2′]iridium(III) 5-methylpyrazinate (dpq)2Ir(mprz) (2), which are both based on the use of 2,3-diphenylqu...detailed

The vibrational assignments of the infrared and Raman spectra of the symmetrically substituted 2,3-DIPHENYLQUINOXALINE (cas 1684-14-6) and its N,N′-dioxide: Experimental and computational study09/24/2019

2,3-diphenylquinoxaline (DPQ) and 2,3-diphenylquinoxaline N,N′-dioxide (DPQDO) (also known as 2,3-diphenylquinoxaline 1,4-dioxide) were synthesized, and their infrared and Raman spectra were measured. The structural stability and the vibrational spectra of the two quinoxaline molecules were inv...detailed

1684-14-6Relevant articles and documents

Green and efficient synthesis of quinoxaline derivatives via ceric ammonium nitrate promoted and in situ aerobic oxidation of α-hydroxy ketones and α-keto oximes in aqueous media

Shaabani, Ahmad,Maleki, Ali

, p. 79 - 81 (2008)

The direct conversion of α-hydroxy ketones and α-keto oximes into quinoxaline derivatives in the presence of a catalytic amount of ceric ammonium nitrate via metal-catalyzed aerobic oxidation followed by in situ trapping with aromatic 1,2-diamines in water as a green and efficient reaction media, is reported.

Comprehensive experimental investigation of mechanically induced 1,4-diazines synthesis in solid state

Oliveira, Paulo F.M.,Haruta, Naoki,Chamayou, Alain,Guidetti, Brigitte,Baltas, Michel,Tanaka, Kazuyoshi,Sato, Tohru,Baron, Michel

, p. 2305 - 2310 (2017)

Compared mechanosynthesis of two condensed 1,4-diazines were investigated in ball milling conditions from o-phenylenediamine. 13C CP-MAS NMR revealed a hemiaminal intermediate for dibenzo[a,c]phenazine synthesis accumulated under mechanical act

2-Iodo benzoic acid: An unconventional precursor for the one pot multi-component synthesis of quinoxaline using organo Cu (II) catalyst

Saha, Bittu,Mitra, Bijeta,Brahmin, Dhiraj,Sinha, Biswajit,Ghosh, Pranab

, p. 3657 - 3663 (2018)

This is the first reported, unconventional, efficient strategy for the synthesis of quinoxaline from 2 to iodo benzoic acid and sodium azide in presence of organo Cu (II) catalyst. Herein, a very simple, versatile one pot multi-component protocol for the synthesis of biologically active compound, quinoxaline has been described via Schmidt reaction and the nucleophilic substitution reaction. The isolated compounds were characterized by 1H NMR, 13C NMR. Our reported organo catalyst was characterized by single crystal XRD, SEM.

Synthesis, characterization and catalytic activity of oxovanadium(IV) complexes of heterocyclic acid hydrazones

Pandey, Manju,Sunaja Devi,Sreeja

, p. 4135 - 4137 (2015)

Two acid hydrazones, furan-2-carbaldehyde nicotinic hydrazone (L1) and furan-2-carbaldehyde benzhydrazone (L2) have been synthesized and they are characterized by elemental analysis, IR, NMR and UV spectral analysis. Oxovanadium(IV) complexes of these two

Biomass into chemicals: One-pot two- and three-step synthesis of quinoxalines from biomass-derived glycols and 1,2-dinitrobenzene derivatives using supported gold nanoparticles as catalysts

Climent,Corma,Hernandez,Hungria,Iborra,Martinez-Silvestre

, p. 118 - 129 (2012)

An efficient and selective one-pot two-step method, for the synthesis of quinoxalines by oxidative coupling of vicinal diols with 1,2-phenylenediamine derivatives, has been developed by using gold nanoparticles supported on nanoparticulated ceria (Au/CeO2) or hydrotalcite (Au/HT) as catalysts and air as oxidant, in the absence of any homogeneous base. Reaction kinetics shows that the reaction controlling step is the oxidation of the diol to α-hydroxycarbonyl compound. Furthermore, a one-pot three-step synthesis of 2-methylquinoxaline starting from 1,2-dinitrobenzene and 1,2-propanediol has been successfully carried out with 98% conversion and 83% global yield to the final product.

Tungstophosphoric acid/mesoporous silicas as suitable catalysts in quinoxaline synthesis

Langer, Peter,Luque, Rafael,Palermo, Valeria,Pizzio, Luis R.,Romanelli, Gustavo P.,Sosa, Alexis A.

, (2021/12/16)

Quinoxalines and their derivatives are of great value in the chemical and biological sciences. These compounds are found in dyes, agrochemicals, and are used as building blocks of drugs for the treatment of different diseases. Quinoxalines and their deriv

Ultrasound/visible light-mediated synthesis of N-heterocycles using g-C3N4/Cu3TiO4 as sonophotocatalyst

Arunachalapandi, Murugan,Roopan, Selvaraj Mohana

, p. 3363 - 3378 (2021/04/19)

In this investigation, novel g-C3N4/Cu3TiO4 (CNCT) nanocomposite was synthesized by using a simple thermal condensation method. The synthesized CNCT nanocomposite was characterized by X-ray Diffraction, Transmission electron microscopy, Atomic force microscopy, Energy-dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, UV–vis diffuse reflectance spectroscopy, Photoluminescence, Brunauer–Emmett–Telle, Zeta Potential, and Thermogravimetric analysis. The study revealed that the catalysts prepared have high crystalline nature, optical light-absorbing property, high surface area, and stability. The CNCT- nanocomposite was found to be an extraordinary visible light absorbing catalyst for the synthesis of quinoxaline and quinazolinone derivatives, which have important benefits in a variety of drug applications. Quinoxaline and quinazolinones were prepared from anthranilamide, diamines, benzil, and corresponding aldehydes under Ultrasonic/visible light-medium with a notable amount of g-C3N4/Cu3TiO4. The results exhibit good and excellent yields of product derivatives at mild conditions under Ultrasonic/visible light-medium. Ultrasounds always clean the active site catalyst, promoting activity and reusability. Most notably, with preserved reactivities, this heterogeneous g-C3N4/Cu3TiO4 composite can be used atleast 5 times. Furthermore, we examined the reusability of the catalyst under Ultrasonication coupled with Visible light and in the absence of an Ultrasonication medium. Finally, advantages of the method are non-conventional approach, green solvent, reduced reaction duration, mild condition, and reusable catalyst.

BSA-encapsulated cyclometalated iridium complexes as nano-photosensitizers for photodynamic therapy of tumor cells

Xu, Yao,Wang, Xiang,Song, Kang,Du, Jun,Liu, Jinliang,Miao, Yuqing,Li, Yuhao

, p. 15323 - 15331 (2021/05/19)

Photodynamic therapy is a promising treatment method. The development of suitable photosensitizers can improve therapeutic efficacy. Herein, we report three iridium complexes (Ir1, Ir2, and Ir3), and encapsulate them within bovine serum albumin (BSA) to f

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