Benzenamine, 4,4'-(bromoethenylidene)bis-

Base Information

Chemical Name:Benzenamine, 4,4'-(bromoethenylidene)bis-
CAS No.:56138-91-1
Molecular Formula:C₁₄H₁₃BrN₂
Molecular Weight:289.175
Hs Code.:
DSSTox Substance ID:DTXSID20204669

Synonyms:BRN 2729677;Benzenamine, 4,4'-(bromoethenylidene)bis-;4,4'-(Bromoethenylidene)bisbenzenamine;1,1-Bis(p-aminophenyl)-2-bromoethylene;56138-91-1;C14H13BrN2;DTXSID20204669;LS-28127

Suppliers and Price of Benzenamine, 4,4'-(bromoethenylidene)bis-

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 Benzenamine, 4,4'-(bromoethenylidene)bis-

Chemical Property:

XLogP3:3.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:288.02621
Heavy Atom Count:17
Complexity:237

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1C(=CBr)C2=CC=C(C=C2)N)N

Technology Process of Benzenamine, 4,4'-(bromoethenylidene)bis-

There total 3 articles about Benzenamine, 4,4'-(bromoethenylidene)bis- 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:

: 56138-85-3
1,1'-(2,2-dibromo-1,1-ethanediyl)dibenzene

: 56138-91-1
C₁₄H₁₃BrN₂

Guidance literature:: Multi-step reaction with 3 steps

1: HNO₃

2: SnCl₂, aq. HCl

3: KOH / ethanol

With hydrogenchloride; potassium hydroxide; nitric acid; tin(ll) chloride; In ethanol;

Reference yield:

: 56138-84-2
1,1-dibromo-2,2-bis(4-nitrophenyl)ethane

: 56138-91-1
C₁₄H₁₃BrN₂

Guidance literature:: Multi-step reaction with 2 steps

1: SnCl₂, aq. HCl

2: KOH / ethanol

With hydrogenchloride; potassium hydroxide; tin(ll) chloride; In ethanol;