4-Nitro-N,N'-diphenylbenzenecarboximidamide

Base Information

• Chemical Name: 4-Nitro-N,N'-diphenylbenzenecarboximidamide
• CAS No.: 19555-22-7
• Molecular Formula: C19H15N3O2
• Molecular Weight: 317.347
• NSC Number: 143508
• DSSTox Substance ID: DTXSID70941335
• Nikkaji Number: J1.449.174K
• ChEMBL ID: CHEMBL56231

Synonyms:19555-22-7;4-Nitro-N,N'-diphenylbenzenecarboximidamide;Amidine deriv.;4-Nitro-N,N'-diphenyl-benzamidine;NSC143508;CHEMBL56231;SCHEMBL9804137;DTXSID70941335;NSC-143508;4-Nitro-N,N'-diphenylbenzene-1-carboximidamide

Chemical Property of 4-Nitro-N,N'-diphenylbenzenecarboximidamide

Chemical Property:

• Boiling Point: 510.6°Cat760mmHg
• Flash Point: 262.6°C
• Density: 1.18g/cm³
• XLogP3: 4.4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 317.116426730
• Heavy Atom Count: 24
• Complexity: 426

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

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

Technology Process of 4-Nitro-N,N'-diphenylbenzenecarboximidamide

There total 8 articles about 4-Nitro-N,N'-diphenylbenzenecarboximidamide 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: 89.0%

4-nitrobenzanilide (3460-11-5) + aniline (62-53-3) → 4-nitro-N,N'-diphenyl-benzamidine (19555-22-7)

Guidance literature:

4-nitrobenzanilide; With magnesia; In neat (no solvent); at 70 ℃; for 0.5h;

aniline; In neat (no solvent); at 70 ℃; for 5h;

DOI:10.1016/j.tetlet.2013.05.096

Reference yield: 84.0%

aniline (62-53-3) + 4-nitro-benzoic acid (62-23-7) → N,N'-diphenyl-4-nitrobenzenecarboximidamide (19555-22-7)

Guidance literature:

With PPSE; at 160 ℃; for 5h;

DOI:10.1246/bcsj.59.2171

Reference yield: 6.0%

(E)-N-(4-nitrobenzylidene)aniline (1614-00-2) + phenylacetylene (536-74-3) → 2-(4-nitrophenyl)-4-phenylquinoline (1049-08-7) + N,N'-diphenyl-4-nitrobenzenecarboximidamide (19555-22-7)

Guidance literature:

With iron(III) chloride; chloranil; In acetonitrile; for 0.5h; Heating;

DOI:10.1021/jo00032a043

upstream raw materials:

aniline hydrochloride

4-Nitro-N-phenyl-benzimidoyl chloride

aniline

4-nitro-benzoic acid

Downstream raw materials:

4-amino-N,N'-diphenyl-benzamidine

N¹-(2-Benzyl-5,6,7,8-tetrachlor-2,3-dihydro-3-oxo-1,4-benzodioxin-2-ylcarbonyl)-4-nitro-N¹,N²-diphenylbenzamidin

4-Nitro-N¹,N²-diphenyl-N¹-(5,6,7,8-tetrachlor-2-ethyl-2,3-dihydro-3-oxo-1,4-benzodioxin-2-ylcarbonyl)benzamidin

N¹-Isobutyryl-4-nitro-N¹,N²-diphenylbenzamidin

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