4-amino-1-(N-ethylamino)benzene

Base Information

• Chemical Name: 4-amino-1-(N-ethylamino)benzene
• CAS No.: 5840-09-5
• Molecular Formula: C8H12N2
• Molecular Weight: 136.197
• Hs Code.: 2921590090
• European Community (EC) Number: 845-563-0
• Nikkaji Number: J28.423H
• Mol file: 5840-09-5.mol

Synonyms:5840-09-5;N-Ethyl-p-phenylenediamine;4-amino-1-(N-ethylamino)benzene;4-N-ethylbenzene-1,4-diamine;1-N-ethylbenzene-1,4-diamine;Monoathyl-p-phenylendiamin;N1-ethylbenzene-1,4-diamine;SCHEMBL146408;AKOS005350654;EN300-80358;Z359511474

Chemical Property of 4-amino-1-(N-ethylamino)benzene

Chemical Property:

• PSA: 38.05000
• LogP: 2.35480
• XLogP3: 1.2
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 136.100048391
• Heavy Atom Count: 10
• Complexity: 85.3

Purity/Quality:

99.90% ^*data from raw suppliers

4-Amino-1-(N-ethylamino)benzene ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCNC1=CC=C(C=C1)N

Technology Process of 4-amino-1-(N-ethylamino)benzene

There total 15 articles about 4-amino-1-(N-ethylamino)benzene 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: 99.0%

2-[(4-ethylaminophenylamino)methylene]malonic acid diethyl ester (1222062-40-9) → 4-amino-1-(N-ethylamino)benzene (5840-09-5)

Guidance literature:

With ethylenediamine; In ethanol; at 20 ℃; for 0.25h;

DOI:10.1002/chem.200902054

Reference yield: 75.0%

4-nitroso-N-ethylaniline (19788-30-8) → 4-amino-1-(N-ethylamino)benzene (5840-09-5)

Guidance literature:

With ammonium chloride; aluminium; In methanol; for 6h; Heating;

Reference yield:

(4-ethylamino-phenylimino)-phenyl-acetonitrile → benzoyl cyanide (613-90-1) + 4-amino-1-(N-ethylamino)benzene (5840-09-5)

Guidance literature:

upstream raw materials:

N-nitroso N-ethyl-N-(4-nitroaniline)

4-nitroso-N-ethylaniline

hydrogenchloride

N-ethyl-N-nitrosoaniline

Downstream raw materials:

N-[2-(4-Ethylamino-phenylamino)-5-hydroxy-4-methyl-phenyl]-acetamide

1-[2,3-di(tert-butoxycarbonyl)guanidino]-4-(N-ethyl)benzene

2-(4-ethylamino-phenylimino)-imidazolidine-1,3-dicarboxylic acid di-tert-butyl ester

N-[1,3-di(tert-butoxycarbonyl)-4-(fur-2-yl)imidazolidin-2-ylidene]-4-ethylaminoaniline