N1,N4,N4-Trimethyl-2-nitro-1,4-benzenediamine

Base Information

Chemical Name:N1,N4,N4-Trimethyl-2-nitro-1,4-benzenediamine
CAS No.:16293-15-5
Molecular Formula:C₉H₁₃N₃O₂
Molecular Weight:195.221
Hs Code.:
DSSTox Substance ID:DTXSID301250704

Synonyms:N1,N4,N4-Trimethyl-2-nitro-1,4-benzenediamine;DTXSID301250704;16293-15-5

Suppliers and Price of N1,N4,N4-Trimethyl-2-nitro-1,4-benzenediamine

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 0 raw suppliers

Chemical Property of N1,N4,N4-Trimethyl-2-nitro-1,4-benzenediamine

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:195.100776666
Heavy Atom Count:14
Complexity:203

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CNC1=C(C=C(C=C1)N(C)C)[N+](=O)[O-]

Technology Process of N1,N4,N4-Trimethyl-2-nitro-1,4-benzenediamine

There total 3 articles about N1,N4,N4-Trimethyl-2-nitro-1,4-benzenediamine 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:

: 85020-97-9
N-(4-Dimethylamino-2-nitro-phenyl)-N-methyl-acetamide

: 16293-15-5
4-N,N-dimethylamino-N-methyl-2-nitroaniline

Guidance literature:: With potassium hydroxide; In ethanol; water; for 1h; Yield given; Heating;

Reference yield:

: 29124-72-9
4-N,N-dimethylamino-2-nitroacetanilide

: 16293-15-5
4-N,N-dimethylamino-N-methyl-2-nitroaniline

Guidance literature:: Multi-step reaction with 2 steps

1: KOH / acetone / 0.5 h / Heating

2: potassium hydroxide / ethanol; H₂O / 1 h / Heating

With potassium hydroxide; In ethanol; water; acetone;