9-Nitroacenaphtho[1,2-b]quinoxaline

Base Information

Chemical Name:9-Nitroacenaphtho[1,2-b]quinoxaline
CAS No.:134859-12-4
Molecular Formula:C₁₈H₉N₃O₂
Molecular Weight:299.288
Hs Code.:
European Community (EC) Number:654-587-9
NSC Number:163379
Pharos Ligand ID:SCNR6DWNNR1D
ChEMBL ID:CHEMBL3217889

Synonyms:9-nitroacenaphtho[1,2-b]quinoxaline;134859-12-4;9-nitroacenaphthyleno[1,2-b]quinoxaline;NSC 163379;9-NITROACENAPHTHO(1,2-B)QUINOXALINE;NSC163379;Acenaphtho[1, 9-nitro-;CBDivE_010071;CHEMBL3217889;STK862841;AKOS000733180;NSC-163379;EN300-18205510;Z55723204

Suppliers and Price of 9-Nitroacenaphtho[1,2-b]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
Packaging
price

TRC
7-Nitro-3,10-Diazapentacyclo[10.7.1.0^{2,11}.0^{4,9}.0^{16,20}]Icosa-1(20),2,4(9),5,7,10,12,14,16,18-decaene
1g
$ 65.00

Total 4 raw suppliers

Chemical Property of 9-Nitroacenaphtho[1,2-b]quinoxaline

Chemical Property:

Melting Point:>300 °C(Solv: ethanol (64-17-5))
Boiling Point:568.5±30.0 °C(Predicted)
Density:1.539±0.06 g/cm3(Predicted)
XLogP3:3.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:0
Exact Mass:299.069476538
Heavy Atom Count:23
Complexity:493

Purity/Quality:

85.0-99.8% ^*data from raw suppliers

7-Nitro-3,10-Diazapentacyclo[10.7.1.0^{2,11}.0^{4,9}.0^{16,20}]Icosa-1(20),2,4(9),5,7,10,12,14,16,18-decaene ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC2=C3C(=C1)C4=NC5=C(C=C(C=C5)[N+](=O)[O-])N=C4C3=CC=C2

Technology Process of 9-Nitroacenaphtho[1,2-b]quinoxaline

There total 1 articles about 9-Nitroacenaphtho[1,2-b]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: 98.0%

: 99-56-9
4-Nitrophenylene-1,2-diamine

: 82-86-0
acenaphthene quinone

: 134859-12-4
9-nitro-acenaphtho[1,2-b]quinoxaline

Guidance literature:: With 1-(propyl-3-sulfonate) 3-methylimidazol(3H)-1-ium phosphotungstate; In water; at 20 ℃; for 0.116667h; Reagent/catalyst; Time;
DOI:10.2174/1386207311316080004