N-(4-Fluorobenzylidene)-para-toluidine

Base Information

Chemical Name:N-(4-Fluorobenzylidene)-para-toluidine
CAS No.:39769-11-4
Molecular Formula:C14H12FN
Molecular Weight:213.254
Hs Code.:
European Community (EC) Number:651-950-3
Nikkaji Number:J994.466D
Mol file:39769-11-4.mol

Synonyms:N-(4-fluorobenzylidene)-4-methylaniline;N-(4-FLUOROBENZYLIDENE)-PARA-TOLUIDINE;AKOS001055848;AKOS024333578;AB00719889-01;N-[(4-fluorophenyl)methylidene]-4-methylaniline;Z53773455

Suppliers and Price of N-(4-Fluorobenzylidene)-para-toluidine

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 1 raw suppliers

Chemical Property of N-(4-Fluorobenzylidene)-para-toluidine

Chemical Property:

XLogP3:3.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:213.095377549
Heavy Atom Count:16
Complexity:223

Purity/Quality:: 98%,99%, ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=C(C=C1)N=CC2=CC=C(C=C2)F

Technology Process of N-(4-Fluorobenzylidene)-para-toluidine

There total 6 articles about N-(4-Fluorobenzylidene)-para-toluidine 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: 96.0%

: 459-57-4
4-fluorobenzaldehyde

: 106-49-0,12221-03-3
p-toluidine

: 39769-11-4
(E)-N-(4-fluorobenzylidene)-4-methylaniline

Guidance literature:: With sulfuric acid; In methanol; water; at 50 ℃; for 0.333333h; Sonication; Green chemistry;
DOI:10.1016/j.molstruc.2018.12.114