3-Nitro-N-(3-((3-nitrobenzoyl)amino)phenyl)benzamide

Base Information

• Chemical Name: 3-Nitro-N-(3-((3-nitrobenzoyl)amino)phenyl)benzamide
• CAS No.: 4233-27-6
• Molecular Formula: C20H14N4O6
• Molecular Weight: 406.34800
• Hs Code.: 2924299090
• European Community (EC) Number: 670-131-1
• Mol file: 4233-27-6.mol

Synonyms:3-NITRO-N-(3-((3-NITROBENZOYL)AMINO)PHENYL)BENZAMIDE;AKOS003889493

Chemical Property of 3-Nitro-N-(3-((3-nitrobenzoyl)amino)phenyl)benzamide

Chemical Property:

• PSA: 149.84000
• LogP: 5.20000
• XLogP3: 3.2
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 4
• Exact Mass: 406.09133418
• Heavy Atom Count: 30
• Complexity: 607

Purity/Quality:

95% ^*data from raw suppliers

3-NITRO-N-(3-((3-NITROBENZOYL)AMINO)PHENYL)BENZAMIDE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)NC2=CC(=CC=C2)NC(=O)C3=CC(=CC=C3)[N+](=O)[O-]

Technology Process of 3-Nitro-N-(3-((3-nitrobenzoyl)amino)phenyl)benzamide

There total 2 articles about 3-Nitro-N-(3-((3-nitrobenzoyl)amino)phenyl)benzamide 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: 82.5%

m-phenylenediamine (108-45-2,64554-26-3,76583-20-5) + m-nitrobenzoic acid chloride (121-90-4) → bis-1,3-(3-nitrobenzamido)benzene (4233-27-6)

Guidance literature:

With triethylamine; In tetrahydrofuran; for 12h; Ambient temperature;

Reference yield:

→ bis-1,3-(3-nitrobenzamido)benzene (4233-27-6)

Guidance literature:

entspr. Saeurechlorid, m-Phenylendiamin;

Reference yield: 85.0%

bis-1,3-(3-nitrobenzamido)benzene (4233-27-6) → bis-1,3-(3-aminobenzamido)benzene (2362-23-4)

Guidance literature:

With hydrogenchloride; acetic acid; tin(ll) chloride; for 0.333333h;

upstream raw materials:

m-phenylenediamine

m-nitrobenzoic acid chloride

Downstream raw materials:

bis-1,3-(3-aminobenzamido)benzene

bis-1,3-<3-(guanidinoacetamido)benzamido>benzene dihydrochloride

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