Benzenemethanamine, 4,5-dimethoxy-N-(4-(4-(2-methylphenyl)-1-piperazinyl)phenyl)-2-nitro-

Base Information

Chemical Name:Benzenemethanamine, 4,5-dimethoxy-N-(4-(4-(2-methylphenyl)-1-piperazinyl)phenyl)-2-nitro-
CAS No.:78933-09-2
Molecular Formula:C26H30N4O4
Molecular Weight:462.5408
Hs Code.:
DSSTox Substance ID:DTXSID30229383
Wikidata:Q83109612

Synonyms:BRN 4606380;Benzenemethanamine, 4,5-dimethoxy-N-(4-(4-(2-methylphenyl)-1-piperazinyl)phenyl)-2-nitro-;4,5-Dimethoxy-N-(4-(4-(2-methylphenyl)-1-piperazinyl)phenyl)-2-nitrobenzenemethanamine;78933-09-2;DTXSID30229383;LS-30461

Suppliers and Price of Benzenemethanamine, 4,5-dimethoxy-N-(4-(4-(2-methylphenyl)-1-piperazinyl)phenyl)-2-nitro-

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of Benzenemethanamine, 4,5-dimethoxy-N-(4-(4-(2-methylphenyl)-1-piperazinyl)phenyl)-2-nitro-

Chemical Property:

Vapor Pressure:1.93E-17mmHg at 25°C
Boiling Point:662.9°Cat760mmHg
Flash Point:354.7°C
Density:1.239g/cm³
XLogP3:5.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:7
Exact Mass:462.22670545
Heavy Atom Count:34
Complexity:631

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=CC=C1N2CCN(CC2)C3=CC=C(C=C3)NCC4=CC(=C(C=C4[N+](=O)[O-])OC)OC

Technology Process of Benzenemethanamine, 4,5-dimethoxy-N-(4-(4-(2-methylphenyl)-1-piperazinyl)phenyl)-2-nitro-

There total 5 articles about Benzenemethanamine, 4,5-dimethoxy-N-(4-(4-(2-methylphenyl)-1-piperazinyl)phenyl)-2-nitro- 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: 60.0%

: 78932-98-6
[1-(4,5-Dimethoxy-2-nitro-phenyl)-meth-(E)-ylidene]-[4-(4-o-tolyl-piperazin-1-yl)-phenyl]-amine

: 78933-09-2
(4,5-Dimethoxy-2-nitro-benzyl)-[4-(4-o-tolyl-piperazin-1-yl)-phenyl]-amine

Guidance literature:: With hydrazine hydrate; palladium on activated charcoal; In N,N-dimethyl-formamide; for 12h; Heating;

Reference yield:

: 39512-51-1
1-(o-toluyl)piperazine

: 78933-09-2
(4,5-Dimethoxy-2-nitro-benzyl)-[4-(4-o-tolyl-piperazin-1-yl)-phenyl]-amine

Guidance literature:: Multi-step reaction with 4 steps

1: 70 percent / 48 h / 120 - 140 °C

2: 75 percent / hydrazin hydrate (98 percent) / Raney nickel / dimethylformamide / 10 h / Heating

3: 80 percent / benzene / 8 h / Heating

4: 60 percent / hydrazin hydrate (98 percent) / Pd-C (10 percent) / dimethylformamide / 12 h / Heating

With hydrazine hydrate; palladium on activated charcoal; nickel; In N,N-dimethyl-formamide; benzene;

Reference yield:

: 100-00-5
4-chlorobenzonitrile

: 78933-09-2
(4,5-Dimethoxy-2-nitro-benzyl)-[4-(4-o-tolyl-piperazin-1-yl)-phenyl]-amine

Guidance literature:: Multi-step reaction with 4 steps

1: 70 percent / 48 h / 120 - 140 °C

2: 75 percent / hydrazin hydrate (98 percent) / Raney nickel / dimethylformamide / 10 h / Heating

3: 80 percent / benzene / 8 h / Heating

4: 60 percent / hydrazin hydrate (98 percent) / Pd-C (10 percent) / dimethylformamide / 12 h / Heating

With hydrazine hydrate; palladium on activated charcoal; nickel; In N,N-dimethyl-formamide; benzene;