1,2-Benzenediamine, N,N'-bis[(4-nitrophenyl)methylene]-

Base Information

• Chemical Name: 1,2-Benzenediamine, N,N'-bis[(4-nitrophenyl)methylene]-
• CAS No.: 74661-46-4
• Molecular Formula: C20H14N4O4
• Molecular Weight: 374.356
• European Community (EC) Number: 666-916-3
• DSSTox Substance ID: DTXSID60391062
• Mol file: 74661-46-4.mol

Synonyms:74661-46-4;1,2-Benzenediamine, N,N'-bis[(4-nitrophenyl)methylene]-;DTXSID60391062;AKOS024399280;N~1~,N~2~-bis[(E)-(4-nitrophenyl)methylidene]-1,2-benzenediamine

Chemical Property of 1,2-Benzenediamine, N,N'-bis[(4-nitrophenyl)methylene]-

Chemical Property:

• PSA: 116.36000
• LogP: 6.05060
• XLogP3: 4.2
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 4
• Exact Mass: 374.10150494
• Heavy Atom Count: 28
• Complexity: 530

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C(=C1)N=CC2=CC=C(C=C2)[N+](=O)[O-])N=CC3=CC=C(C=C3)[N+](=O)[O-]

Technology Process of 1,2-Benzenediamine, N,N'-bis[(4-nitrophenyl)methylene]-

There total 4 articles about 1,2-Benzenediamine, N,N'-bis[(4-nitrophenyl)methylene]- 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: 99.0%

benzaldehyde (100-52-7) + 1,2-diamino-benzene (95-54-5) → O2NC6H4CHNC6H4NCHC6H4NO2 (74661-46-4)

Guidance literature:

With sodium chloride; for 2h; Concentration; Mechanism; Milling;

DOI:10.1002/jhet.1113

Reference yield:

4-nitrobenzaldehdye (555-16-8) + 1,2-diamino-benzene (95-54-5) → O2NC6H4CHNC6H4NCHC6H4NO2 (74661-46-4)

Guidance literature:

In tetrahydrofuran;

DOI:10.1016/j.ejmech.2010.11.027

Reference yield:

4-nitrobenzaldehdye (555-16-8) + 1,2-diamino-benzene (95-54-5) → O2NC6H4CHNC6H4NCHC6H4NO2 (74661-46-4) + 2-(4-nitrophenyl)benzimidazole (729-13-5) + 1-(4-nitrobenzyl)-2-(4-nitrophenyl)-1H-benzimidazole (54821-03-3)

Guidance literature:

With γ-maghemite-silica nanocomposite from 50-150 mg FeCl3/g silica activated; In neat (no solvent); Green chemistry;

DOI:10.1016/j.catcom.2013.06.026

upstream raw materials:

4-nitrobenzaldehdye

1,2-diamino-benzene

benzaldehyde

Downstream raw materials:

2-(4-nitrophenyl)benzimidazole

1-(4-nitrobenzyl)-2-(4-nitrophenyl)-1H-benzimidazole

4-nitrobenzaldehdye

1,2-diamino-benzene