Benzamide, N,N-bis([1,1'-biphenyl]-4-yl)-

Base Information

Chemical Name:Benzamide, N,N-bis([1,1'-biphenyl]-4-yl)-
CAS No.:741267-16-3
Molecular Formula:C31H23NO
Molecular Weight:425.53
Hs Code.:
DSSTox Substance ID:DTXSID20474840
Wikidata:Q82304975

Synonyms:Benzamide, N,N-bis([1,1'-biphenyl]-4-yl)-;741267-16-3;SCHEMBL3933240;DTXSID20474840

Suppliers and Price of Benzamide, N,N-bis([1,1'-biphenyl]-4-yl)-

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,N-bis([1,1'-biphenyl]-4-yl)-

Chemical Property:

XLogP3:7.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:5
Exact Mass:425.177964357
Heavy Atom Count:33
Complexity:544

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=CC=C(C=C2)N(C3=CC=C(C=C3)C4=CC=CC=C4)C(=O)C5=CC=CC=C5

Technology Process of Benzamide, N,N-bis([1,1'-biphenyl]-4-yl)-

There total 2 articles about Benzamide, N,N-bis([1,1'-biphenyl]-4-yl)- 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: 49.0%

: 1591-31-7
4-iodo-biphenyl

: 55-21-0,27208-38-4
benzamide

: 741267-16-3
N,N-di([1,1'-biphenyl]-4-yl)benzamide

: 20743-57-1
N-([1,1'-biphenyl]-4-yl)benzamide

Guidance literature:: With bis(tetrapropylammonium) tetraiododicuprate(I); trans-N,N'-dimethyl-1,2-cyclohexanediamine bis-(methanesulfonic acid); caesium carbonate; In 1,4-dioxane; at 130 ℃; for 24h; Overall yield = 70 %; Overall yield = 402 mg; Inert atmosphere;
DOI:10.1021/jo300905w