N-(4-methylphenyl)-1-(2-nitrophenyl)methanimine

Base Information Edit

Chemical Name:N-(4-methylphenyl)-1-(2-nitrophenyl)methanimine
CAS No.:17064-82-3
Molecular Formula:C14H12N2O2
Molecular Weight:240.261
Hs Code.:
European Community (EC) Number:667-300-7
DSSTox Substance ID:DTXSID50355259
Nikkaji Number:J2.356.709A
Mol file:17064-82-3.mol

Synonyms:17064-82-3;N-(4-methylphenyl)-1-(2-nitrophenyl)methanimine;N-(2-NITROBENZYLIDENE)-P-TOLUIDINE;4-methyl-N-(2-nitrobenzylidene)aniline;SCHEMBL2139660;SCHEMBL2139662;DTXSID50355259;YKRSQWCMPJDBOD-UHFFFAOYSA-N;STK075387;AKOS000484254;4-methyl-N-[(E)-(2-nitrophenyl)methylidene]aniline;(E)-N-(4-Methylphenyl)-1-(2-nitrophenyl)methanimine

Suppliers and Price of N-(4-methylphenyl)-1-(2-nitrophenyl)methanimine

Supply Marketing:Edit

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
N-(2-NITROBENZYLIDENE)-P-TOLUIDINE Aldrich
250mg
$ 144.00

Aronis compounds
(4-methylphenyl)(2-nitrobenzylidene)amine
5mg
$ 15.00

Total 3 raw suppliers

Chemical Property of N-(4-methylphenyl)-1-(2-nitrophenyl)methanimine Edit

Chemical Property:

Melting Point:75 °C
Boiling Point:55 °C(Press: 0.1 Torr)
PKA:2.88±0.50(Predicted)
PSA：58.18000
Density:1.14±0.1 g/cm3(Predicted)
LogP:4.17700
XLogP3:3.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:240.089877630
Heavy Atom Count:18
Complexity:303

Purity/Quality:

99% ^*data from raw suppliers

N-(2-NITROBENZYLIDENE)-P-TOLUIDINE Aldrich ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC=C(C=C1)N=CC2=CC=CC=C2[N+](=O)[O-]

Technology Process of N-(4-methylphenyl)-1-(2-nitrophenyl)methanimine

There total 2 articles about N-(4-methylphenyl)-1-(2-nitrophenyl)methanimine 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: 100.0%