1-(4-Aminophenyl)-3-(4-bromophenyl)prop-2-en-1-one

Base Information

Chemical Name:1-(4-Aminophenyl)-3-(4-bromophenyl)prop-2-en-1-one
CAS No.:26128-65-4
Molecular Formula:C15H12BrNO
Molecular Weight:302.17
Hs Code.:
DSSTox Substance ID:DTXSID80695650

Synonyms:26128-65-4;4-bromo-4'-aminochalcone;DTXSID80695650;VQJUBRITHVAKHO-UHFFFAOYSA-N;1-(4-Aminophenyl)-3-(4-bromophenyl)prop-2-en-1-one

Suppliers and Price of 1-(4-Aminophenyl)-3-(4-bromophenyl)prop-2-en-1-one

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 1-(4-Aminophenyl)-3-(4-bromophenyl)prop-2-en-1-one

Chemical Property:

XLogP3:3.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:301.01023
Heavy Atom Count:18
Complexity:300

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of 1-(4-Aminophenyl)-3-(4-bromophenyl)prop-2-en-1-one

There total 4 articles about 1-(4-Aminophenyl)-3-(4-bromophenyl)prop-2-en-1-one 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: 56.1%

: 13909-51-8
3-(4-bromophenyl)-1-(4-nitrophenyl)prop-2-en-1-one

: 26128-65-4
4-bromo-4'-aminochalcone

Guidance literature:: With tin(ll) chloride; In ethanol; for 1h; Heating / reflux;

Reference yield:

: 99-92-3
p-aminobenzophenone

: 1122-91-4
4-bromo-benzaldehyde

: 26128-65-4
4-bromo-4'-aminochalcone

Guidance literature:: With sodium hydroxide; In ethanol; at 20 ℃; for 12h;
DOI:10.1002/cjoc.201600568

Reference yield:

: 100-19-6
(4-nitrophenyl)ethanone

: 26128-65-4
4-bromo-4'-aminochalcone

Guidance literature:: Multi-step reaction with 2 steps

1: aq. NaOH

2: SnCl₂, aq. HCl, AcOH

With hydrogenchloride; sodium hydroxide; acetic acid; tin(ll) chloride;