(e)-4-Ethoxy-n-(4-nitrobenzylidene)aniline

Base Information

Chemical Name:(e)-4-Ethoxy-n-(4-nitrobenzylidene)aniline
CAS No.:15485-31-1
Molecular Formula:C₁₅H₁₄N₂O₃
Molecular Weight:270.288
Hs Code.:
DSSTox Substance ID:DTXSID901235986
Nikkaji Number:J2.531.123J

Synonyms:15485-31-1;(e)-4-ethoxy-n-(4-nitrobenzylidene)aniline;(E)-N-(4-Ethoxyphenyl)-1-(4-nitrophenyl)methanimine;SCHEMBL9354314;DTXSID901235986;AKOS001581818;(4-ethoxyphenyl)(4-nitrobenzylidene)amine;N-(4-Ethoxyphenyl)-4-nitrobenzenemethaneimine;4-Ethoxy-N-[(4-nitrophenyl)methylene]benzenamine;(E)-4-Ethoxy-N-(4-nitrobenzylidene)aniline, AldrichCPR;N-(4-ethoxyphenyl)-N-[(1E)-(4-nitrophenyl)methylene]amine

Suppliers and Price of (e)-4-Ethoxy-n-(4-nitrobenzylidene)aniline

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

Sigma-Aldrich
(E)-4-Ethoxy-N-(4-nitrobenzylidene)aniline AldrichCPR
1g
$ 258.00

Absolute Chiral
(E)-4-ethoxy-N-(4-nitrobenzylidene)aniline 95%
1 g
$ 178.00

Absolute Chiral
(E)-4-ethoxy-N-(4-nitrobenzylidene)aniline 95%
500 mg
$ 98.00

Total 4 raw suppliers

Chemical Property of (e)-4-Ethoxy-n-(4-nitrobenzylidene)aniline

Chemical Property:

Melting Point:123.5 °C
Boiling Point:441.9±30.0 °C(Predicted)
Density:1.16±0.1 g/cm3(Predicted)
XLogP3:3.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:270.10044231
Heavy Atom Count:20
Complexity:325

Purity/Quality:

98%,99%, ^*data from raw suppliers

(E)-4-Ethoxy-N-(4-nitrobenzylidene)aniline AldrichCPR ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCOC1=CC=C(C=C1)N=CC2=CC=C(C=C2)[N+](=O)[O-]

Technology Process of (e)-4-Ethoxy-n-(4-nitrobenzylidene)aniline

There total 2 articles about (e)-4-Ethoxy-n-(4-nitrobenzylidene)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: 97.0%