(1E)-N-(4-Ethoxyphenyl)-1-phenylethan-1-imine

Base Information

Chemical Name:(1E)-N-(4-Ethoxyphenyl)-1-phenylethan-1-imine
CAS No.:20768-50-7
Molecular Formula:C16H17NO
Molecular Weight:239.317
Hs Code.:
DSSTox Substance ID:DTXSID40574553

Synonyms:20768-50-7;(1E)-N-(4-Ethoxyphenyl)-1-phenylethan-1-imine;DTXSID40574553

Suppliers and Price of (1E)-N-(4-Ethoxyphenyl)-1-phenylethan-1-imine

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
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price

Total 0 raw suppliers

Chemical Property of (1E)-N-(4-Ethoxyphenyl)-1-phenylethan-1-imine

Chemical Property:

XLogP3:3.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:239.131014166
Heavy Atom Count:18
Complexity:260

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC1=CC=C(C=C1)N=C(C)C2=CC=CC=C2

Technology Process of (1E)-N-(4-Ethoxyphenyl)-1-phenylethan-1-imine

There total 2 articles about (1E)-N-(4-Ethoxyphenyl)-1-phenylethan-1-imine 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:

: 98-86-2
acetophenone

: 156-43-4
4-Ethoxyaniline

: 20768-50-7
p-ethoxyanil of acetophenone

Guidance literature:

Reference yield:

: 20768-50-7
p-ethoxyanil of acetophenone

Guidance literature:: Verb.8, p-Phenetidin;
DOI:10.1021/jo00961a024

Reference yield: 95.0%

: 20768-50-7
p-ethoxyanil of acetophenone

: (S)-4-ethoxy-N-(1-phenylethyl)aniline

Guidance literature:: With 3,3'-bis[(1R,2S-2-hydroxy-1,2-diphenylethyl)aminocarbonyl]-9,9'-dimethyl-9H,9'H-1,1'-bipyrido[3,4-b]indole-2-oxide; trichlorosilane; In chloroform; at 27 ℃; for 4h; enantioselective reaction; Inert atmosphere;
DOI:10.1016/j.tet.2013.06.081