2,2'-(Diselane-1,2-diyl)bis[N-(4-nitrophenyl)benzamide]

Base Information

• Chemical Name: 2,2'-(Diselane-1,2-diyl)bis[N-(4-nitrophenyl)benzamide]
• CAS No.: 106663-60-9
• Molecular Formula: C26H18N4O6Se2
• Molecular Weight: 640.372
• DSSTox Substance ID: DTXSID60546398
• Wikidata: Q82424229
• Mol file: 106663-60-9.mol

Synonyms:106663-60-9;SCHEMBL10519516;2,2'-(Diselane-1,2-diyl)bis[N-(4-nitrophenyl)benzamide];DTXSID60546398

Chemical Property of 2,2'-(Diselane-1,2-diyl)bis[N-(4-nitrophenyl)benzamide]

Chemical Property:

• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 7
• Exact Mass: 641.95568
• Heavy Atom Count: 38
• Complexity: 769

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C(=C1)C(=O)NC2=CC=C(C=C2)[N+](=O)[O-])[Se][Se]C3=CC=CC=C3C(=O)NC4=CC=C(C=C4)[N+](=O)[O-]

Technology Process of 2,2'-(Diselane-1,2-diyl)bis[N-(4-nitrophenyl)benzamide]

There total 5 articles about 2,2'-(Diselane-1,2-diyl)bis[N-(4-nitrophenyl)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: 22.0%

2-(4-nitrophenyl)-1,2-benzoisoselenazole-3(2H)-one (81743-92-2) → 2,2‘-diselenobis[N-(4-nitrophenyl)benzamide] (106663-60-9)

Guidance literature:

2-(4-nitrophenyl)-1,2-benzoisoselenazole-3(2H)-one; With methanol; sodium tetrahydroborate; at 0 ℃; for 1h; Inert atmosphere;

In water; for 1h;

DOI:10.24820/ark.5550190.p010.311

Reference yield:

2-(chloroseleno)benzoyl chloride (1441-85-6) → 2,2‘-diselenobis[N-(4-nitrophenyl)benzamide] (106663-60-9)

Guidance literature:

Multi-step reaction with 2 steps

1.1: triethylamine / dichloromethane / 24 h / 20 °C

2.1: sodium tetrahydroborate; methanol / 1 h / 0 °C / Inert atmosphere

2.2: air / 1 h

With methanol; sodium tetrahydroborate; triethylamine; In dichloromethane;

DOI:10.24820/ark.5550190.p010.311

Reference yield:

2,2'-diselanediyl-di-benzoic acid (6512-83-0) → 2,2‘-diselenobis[N-(4-nitrophenyl)benzamide] (106663-60-9)

Guidance literature:

Multi-step reaction with 3 steps

1.1: thionyl chloride / 3 h / 85 °C

2.1: triethylamine / dichloromethane / 24 h / 20 °C

3.1: sodium tetrahydroborate; methanol / 1 h / 0 °C / Inert atmosphere

3.2: air / 1 h

With methanol; sodium tetrahydroborate; thionyl chloride; triethylamine; In dichloromethane;

DOI:10.24820/ark.5550190.p010.311

upstream raw materials:

2-(4-nitrophenyl)-1,2-benzoisoselenazole-3(2H)-one

2,2'-diselanediyl-di-benzoic acid

2-(chloroseleno)benzoyl chloride

anthranilic acid