2,4-Dibromo-N-(4-bromophenyl)-N-(2,4-dibromophenyl)aniline

Base Information

Chemical Name:2,4-Dibromo-N-(4-bromophenyl)-N-(2,4-dibromophenyl)aniline
CAS No.:73087-81-7
Molecular Formula:C18H10Br5N
Molecular Weight:639.804
Hs Code.:
DSSTox Substance ID:DTXSID40557624
Nikkaji Number:J1.300.284C
Wikidata:Q82439580

Synonyms:2,4-Dibromo-N-(4-bromophenyl)-N-(2,4-dibromophenyl)aniline;73087-81-7;SCHEMBL9805842;DTXSID40557624;G66119

Suppliers and Price of 2,4-Dibromo-N-(4-bromophenyl)-N-(2,4-dibromophenyl)aniline

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of 2,4-Dibromo-N-(4-bromophenyl)-N-(2,4-dibromophenyl)aniline

Chemical Property:

XLogP3:8.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:638.66891
Heavy Atom Count:24
Complexity:375

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1N(C2=C(C=C(C=C2)Br)Br)C3=C(C=C(C=C3)Br)Br)Br

Technology Process of 2,4-Dibromo-N-(4-bromophenyl)-N-(2,4-dibromophenyl)aniline

There total 1 articles about 2,4-Dibromo-N-(4-bromophenyl)-N-(2,4-dibromophenyl)aniline 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: 41.9%

: 3310-62-1
2,3-diazabicyclo[2.2.2]oct-2-ene

: 78065-12-0
tris(4-bromophenyl)ammoniumyl hexafluoroantimonate

: 4316-58-9
tri(p-bromophenyl)amine

: 73087-80-6
2,4-dibromophenyl-bis(4'-bromophenyl)amine

: 73087-81-7
bis(2,4-dibromophenyl)-4-bromphenylamine

: C₂₄H₂₂Br₂N₃⁽¹⁺⁾*F₆Sb^(1-)

Guidance literature:: With 2,6-di-tert-butyl-pyridine; In acetonitrile; at 25 ℃; Product distribution; Mechanism; further cation radical reagent; novel oxaditive azoalkane reaction;
DOI:10.1021/ja00231a051