Benzamide, N-phenyl-2-[(phenylmethyl)seleno]-

Base Information

Chemical Name:Benzamide, N-phenyl-2-[(phenylmethyl)seleno]-
CAS No.:126543-42-8
Molecular Formula:C20H17NOSe
Molecular Weight:366.321
Hs Code.:
DSSTox Substance ID:DTXSID90432992
Nikkaji Number:J851.960I
Wikidata:Q82247134
ChEMBL ID:CHEMBL376704
Mol file:126543-42-8.mol

Synonyms:Benzamide, N-phenyl-2-[(phenylmethyl)seleno]-;126543-42-8;CHEMBL376704;SCHEMBL8356827;DTXSID90432992;N-Phenyl-2-(benzylseleno)benzamide

Suppliers and Price of Benzamide, N-phenyl-2-[(phenylmethyl)seleno]-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 1 raw suppliers

Chemical Property of Benzamide, N-phenyl-2-[(phenylmethyl)seleno]-

Chemical Property:

Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:5
Exact Mass:367.04754
Heavy Atom Count:23
Complexity:361

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C[Se]C2=CC=CC=C2C(=O)NC3=CC=CC=C3

Technology Process of Benzamide, N-phenyl-2-[(phenylmethyl)seleno]-

There total 1 articles about Benzamide, N-phenyl-2-[(phenylmethyl)seleno]- 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: 45.0%

: 93-98-1,5705-51-1
N-phenyl benzoyl amide

: 100-39-0
benzyl bromide

: 126543-42-8
2-benzylseleno-N-phenylbenzamide

Guidance literature:: N-phenyl benzoyl amide; With n-butyllithium; In tetrahydrofuran; hexane; at 0 ℃; for 0.5h;

With selenium; In tetrahydrofuran; hexane; for 0.5h;

benzyl bromide; In tetrahydrofuran; hexane; at 0 - 20 ℃; for 1.5h;
DOI:10.1016/j.bmcl.2006.07.085

Reference yield:

: 27607-77-8
trimethylsilyl trifluoromethanesulfonate

: 126543-42-8
2-benzylseleno-N-phenylbenzamide

: 2-benzylseleno-N-trimethylsilylbenzanilide

Guidance literature:: With triethylamine; In diethyl ether; Ambient temperature;
DOI:10.1071/CH9951221

Reference yield:

: 126543-42-8
2-benzylseleno-N-phenylbenzamide

: 106663-84-7
2,2‘-diselenobis(N-phenylbenzamide)

Guidance literature:: With Perbenzoic acid; 2,2'-azobis(isobutyronitrile); triphenylstannane; Yield given. Multistep reaction; 1.) benzene, reflux; 2.) benzene, reflux;
DOI:10.1016/0040-4039(95)01511-F