2-(4-Nitrophenyl)quinoxaline

Base Information

Chemical Name:2-(4-Nitrophenyl)quinoxaline
CAS No.:5541-64-0
Molecular Formula:C14H9N3O2
Molecular Weight:251.244
Hs Code.:
DSSTox Substance ID:DTXSID901319859
Nikkaji Number:J2.609.891B
ChEMBL ID:CHEMBL1434990

Synonyms:2-(4-nitrophenyl)quinoxaline;5541-64-0;2-(4-Nitro-phenyl)-quinoxaline;Cambridge id 5162291;Oprea1_235725;MLS001203625;SCHEMBL7153742;CHEMBL1434990;DTXSID901319859;HMS2844P16;STK862697;AKOS000578941;CCG-276100;SMR000505095;AB00074752-01

Suppliers and Price of 2-(4-Nitrophenyl)quinoxaline

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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price

Total 1 raw suppliers

Chemical Property of 2-(4-Nitrophenyl)quinoxaline

Chemical Property:

Vapor Pressure:1.8E-07mmHg at 25°C
XLogP3:2.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:251.069476538
Heavy Atom Count:19
Complexity:323

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C2C(=C1)N=CC(=N2)C3=CC=C(C=C3)[N+](=O)[O-]

Technology Process of 2-(4-Nitrophenyl)quinoxaline

There total 24 articles about 2-(4-Nitrophenyl)quinoxaline which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 96.0%

: 99-81-0
4-Nitrophenacyl bromide

: 95-54-5
1,2-diamino-benzene

: 5541-64-0
2-(4-nitro-phenyl)-quinoxaline

Guidance literature:: With 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; In ethyl acetate; at 0 - 20 ℃; for 5h;
DOI:10.1039/c6ra03078e

Reference yield: 95.0%

: 64611-67-2
2-hydroxy-1-(4-nitrophenyl)ethanone

: 95-54-5
1,2-diamino-benzene

: 5541-64-0
2-(4-nitro-phenyl)-quinoxaline

Guidance literature:: With iodine; toluene-4-sulfonic acid; In toluene; at 60 ℃; for 14h; Molecular sieve;
DOI:10.1021/acs.orglett.6b02133

Reference yield: 92.0%

: 100-13-0
4-nitrostyrene

: 95-54-5
1,2-diamino-benzene

: 5541-64-0
2-(4-nitro-phenyl)-quinoxaline

Guidance literature:: 4-nitrostyrene; With tert.-butylhydroperoxide; water; iodine; at 120 ℃; for 1h; Sealed tube;

1,2-diamino-benzene; With dimethyl sulfoxide; at 120 ℃; for 2h; Sealed tube;
DOI:10.1039/c4ra08589b