N-(9H-Fluoren-9-ylidene)-4-(trifluoromethyl)aniline

Base Information

Chemical Name:N-(9H-Fluoren-9-ylidene)-4-(trifluoromethyl)aniline
CAS No.:68161-28-4
Molecular Formula:C₂₀H₁₂F₃N
Molecular Weight:323.317
Hs Code.:
European Community (EC) Number:661-280-3

Synonyms:N-(9H-Fluoren-9-ylidene)-4-(trifluoromethyl)aniline;68161-28-4;AKOS024340775

Suppliers and Price of N-(9H-Fluoren-9-ylidene)-4-(trifluoromethyl)aniline

Supply Marketing:

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

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Chemical Property of N-(9H-Fluoren-9-ylidene)-4-(trifluoromethyl)aniline

Chemical Property:

XLogP3:6.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:323.09218387
Heavy Atom Count:24
Complexity:452

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C3=CC=CC=C3C2=NC4=CC=C(C=C4)C(F)(F)F

Technology Process of N-(9H-Fluoren-9-ylidene)-4-(trifluoromethyl)aniline

There total 1 articles about N-(9H-Fluoren-9-ylidene)-4-(trifluoromethyl)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:

: 68161-28-4
Fluoren-9-ylidene-(4-trifluoromethyl-phenyl)-amine

Guidance literature:: Fluorenon, p-Trifluormethylanilin, BF3-Etherat;
DOI:10.1002/jps.2600670721

Reference yield:

: 68161-28-4
Fluoren-9-ylidene-(4-trifluoromethyl-phenyl)-amine

: 66783-77-5
4'-tert-butyl-5'-oxo-3'-(4-trifluoromethyl-phenyl)-spiro[fluorene-9,2'-oxazolidine]-4'-carbonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: AcOOH

2: toluene

With peracetic acid; In toluene;
DOI:10.1021/jo01331a002