bis(2-(N-phenylcarboxamido)phenyl)diselenide

Base Information

• Chemical Name: bis(2-(N-phenylcarboxamido)phenyl)diselenide
• CAS No.: 106663-84-7
• Molecular Formula: C26H20 N2 O2 Se2
• Molecular Weight: 550.377
• Hs Code.: 2924299090
• Mol file: 106663-84-7.mol

Synonyms:2,2'-Diselenobis(N-phenylbenzamide);2,2'-Diselenobis(benzanilide); Bis[2-(N-phenylcarbamoyl)phenyl] diselenide;Bis[2-(phenylaminocarbonyl)phenyl] diselenide; Bis[2-(phenylcarbamoyl)phenyl]diselenide; Ebselen diselenide; NSC 639778

Chemical Property of bis(2-(N-phenylcarboxamido)phenyl)diselenide

Chemical Property:

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• PSA: 65.18000
• Density: g/cm³
• LogP: 4.23340

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of bis(2-(N-phenylcarboxamido)phenyl)diselenide

There total 23 articles about bis(2-(N-phenylcarboxamido)phenyl)diselenide 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: 100.0%

2-phenyl-1,2-benzoisoselenazol-3(2H)-one (60940-34-3) → 2,2‘-diselenobis(N-phenylbenzamide) (106663-84-7)

Guidance literature:

With triphenylphosphine;

DOI:10.1039/c0ob01234c

Reference yield: 95.0%

2-phenyl-1,2-benzioselenazol-3(2H)-one selenoxide (104473-83-8) → 2,2‘-diselenobis(N-phenylbenzamide) (106663-84-7)

Guidance literature:

With triphenylphosphine; In dichloromethane; for 4h; Ambient temperature;

Reference yield: 79.0%

N-phenyl-2-(triphenylstannylseleno)benzamide → 2,2‘-diselenobis(N-phenylbenzamide) (106663-84-7)

Guidance literature:

With dibenzoyl peroxide; In benzene; Heating;

DOI:10.1021/jo970019t

upstream raw materials:

N-phenyl benzoyl amide

2-phenyl-1,2-benzoisoselenazol-3(2H)-one

phenylmethanethiol

2-phenyl-1,2-benzioselenazol-3(2H)-one selenoxide

Downstream raw materials:

2-phenyl-1,2-benzoisoselenazol-3(2H)-one

ebselen seleninic acid

2-methylseleno-N-phenylbenzamide

2-phenyl-1,2-benzioselenazol-3(2H)-one selenoxide

Refernces

• 1、 Fong, Mei C.,Gable, Robert W.,Schiesser, Carl H.. "N-phenyl-2-(triphenylstannylseleno)benzamide and 2-methylseleno-N-phenylbenzamide". . p. 1886 - 1889. Retrieved 1996.
• 2、 Macegoniuk, Katarzyna,Grela, Ewa,Palus, Jerzy,Rudzińska, Ewa,Grabowiecka, Agnieszka,Biernat, Monika,Berlicki, ?ukasz. "1,2-Benzisoselenazol-3(2H)-one Derivatives As a New Class of Bacterial Urease Inhibitors". . p. 8125 - 8133. Retrieved 2016/10/20.
• 3、 Wang, Zhiren,Wang, Yali,Li, Wenrui,Liu, Zhihong,Luo, Zonghua,Sun, Yang,Wu, Ruibo,Huang, Ling,Li, Xingshu. "Computer-assisted designed "selenoxy-chinolin": A new catalytic mechanism of the GPx-like cycle and inhibition of metal-free and metal-associated Aβ aggregation". supporting information. p. 20913 - 20925. Retrieved 2015/12/11.