Benzenamine, 4-methoxy-N-[[4-(trifluoromethyl)phenyl]methylene]-

Base Information

Chemical Name:Benzenamine, 4-methoxy-N-[[4-(trifluoromethyl)phenyl]methylene]-
CAS No.:144465-76-9
Molecular Formula:C₁₅H₁₂F₃NO
Molecular Weight:279.262
Hs Code.:
DSSTox Substance ID:DTXSID40462764
Nikkaji Number:J994.470B

Synonyms:Benzenamine, 4-methoxy-N-[[4-(trifluoromethyl)phenyl]methylene]-;144465-76-9;SCHEMBL7723176;SCHEMBL20871240;DTXSID40462764;PCPNWEZCMFPNNL-VXLYETTFSA-N

Suppliers and Price of Benzenamine, 4-methoxy-N-[[4-(trifluoromethyl)phenyl]methylene]-

Supply Marketing:

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

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Chemical Property of Benzenamine, 4-methoxy-N-[[4-(trifluoromethyl)phenyl]methylene]-

Chemical Property:

XLogP3:4.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:279.08709849
Heavy Atom Count:20
Complexity:314

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC=C(C=C1)N=CC2=CC=C(C=C2)C(F)(F)F

Technology Process of Benzenamine, 4-methoxy-N-[[4-(trifluoromethyl)phenyl]methylene]-

There total 4 articles about Benzenamine, 4-methoxy-N-[[4-(trifluoromethyl)phenyl]methylene]- 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: 92.0%

: 455-19-6
4-Trifluoromethylbenzaldehyde

: 104-94-9
4-methoxy-aniline

: 130632-08-5,144465-76-9
4-methoxy-N-(4-(trifluoromethyl)benzylidene)aniline

Guidance literature:: With magnesium sulfate; In dichloromethane; at 20 ℃; for 0.5h;
DOI:10.1055/s-0029-1218387

Reference yield: 81.0%

: 349-95-1
4-(trifluoromethyl)benzylic alcohol

: 100-17-4
para-methoxynitrobenzene

: 130632-08-5,144465-76-9
4-methoxy-N-(4-(trifluoromethyl)benzylidene)aniline

Guidance literature:: With potassium phosphate monohydrate; trimethylamine-N-oxide; C₁₈H₂₇FeO₄Si₂; In toluene; at 150 ℃; for 24h; Inert atmosphere; Schlenk technique; Sealed tube;
DOI:10.1021/acs.joc.0c02505

Reference yield:

: 79128-84-0
N-(4-chlorophenyl)-1-(4-(trifluoromethyl)phenyl)methanimine

: 130632-08-5,144465-76-9
4-methoxy-N-(4-(trifluoromethyl)benzylidene)aniline

Guidance literature:: Multi-step reaction with 2 steps

1: chloroform-d1; water

2: ethanol / 8 h / Reflux

In chloroform-d1; ethanol; water;
DOI:10.1021/jacs.0c04705