2-(4-Nitrophenyl)-1H-imidazo[4,5-f][1,10]phenanthroline

Base Information

Chemical Name:2-(4-Nitrophenyl)-1H-imidazo[4,5-f][1,10]phenanthroline
CAS No.:185129-92-4
Molecular Formula:C19H11N5O2
Molecular Weight:341.329
Hs Code.:
DSSTox Substance ID:DTXSID001203297
Nikkaji Number:J1.009.808D
Mol file:185129-92-4.mol

Synonyms:185129-92-4;2-(4-Nitrophenyl)-1H-imidazo[4,5-f][1,10]phenanthroline;2-(4-Nitrophenyl)-1H-imidazo[4,5-f][1,10]phenanthrolline;DTXSID001203297;F14638;A900919;2-(4-nitrophenyl)imidazo[4,5-f]-1,10-phenanthroline

Suppliers and Price of 2-(4-Nitrophenyl)-1H-imidazo[4,5-f][1,10]phenanthroline

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

Crysdot
2-(4-Nitrophenyl)-1H-imidazo[4,5-f][1,10]phenanthroline 97%
1g
$ 887.00

Total 6 raw suppliers

Chemical Property of 2-(4-Nitrophenyl)-1H-imidazo[4,5-f][1,10]phenanthroline

Chemical Property:

Melting Point:302 °C
Boiling Point:676.8±65.0 °C(Predicted)
PKA:8.07±0.50(Predicted)
PSA：100.28000
Density:1.504±0.06 g/cm3(Predicted)
LogP:4.75770
XLogP3:3.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:1
Exact Mass:341.09127461
Heavy Atom Count:26
Complexity:533

Purity/Quality:

97% ^*data from raw suppliers

2-(4-Nitrophenyl)-1H-imidazo[4,5-f][1,10]phenanthroline 97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC2=C3C(=C4C=CC=NC4=C2N=C1)N=C(N3)C5=CC=C(C=C5)[N+](=O)[O-]

Technology Process of 2-(4-Nitrophenyl)-1H-imidazo[4,5-f][1,10]phenanthroline

There total 3 articles about 2-(4-Nitrophenyl)-1H-imidazo[4,5-f][1,10]phenanthroline 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: 95.0%

: 27318-90-7
1,10-phenanthroline-5,6-dione

: 555-16-8
4-nitrobenzaldehdye

: 185129-92-4
?2-(4-nitrophenyl)-1H-imidazo[4,5-f][1,10]phenanthroline

Guidance literature:: With ammonium acetate; acetic acid; at 85 ℃; for 2h;
DOI:10.1002/ejic.201701126

Reference yield: 60.0%

: C₁₂H₁₀N₂O₂

: 555-16-8
4-nitrobenzaldehdye

: 185129-92-4
?2-(4-nitrophenyl)-1H-imidazo[4,5-f][1,10]phenanthroline

Guidance literature:: With hydrogenchloride; ammonium chloride; In water; Reflux;

Reference yield:

: 66-71-7
1,10-Phenanthroline

: 185129-92-4
?2-(4-nitrophenyl)-1H-imidazo[4,5-f][1,10]phenanthroline

Guidance literature:: Multi-step reaction with 2 steps

1: sodium bromide; sulfuric acid; nitric acid / 4.08 h / 85 °C

2: ammonium acetate; acetic acid / Reflux

With sulfuric acid; ammonium acetate; nitric acid; acetic acid; sodium bromide;
DOI:10.1039/c3nj00826f