Benzamide, p-amino-N-(o-((diethylamino)methyl)benzyl)-

Base Information

Chemical Name:Benzamide, p-amino-N-(o-((diethylamino)methyl)benzyl)-
CAS No.:84227-74-7
Molecular Formula:C19H25 N3 O
Molecular Weight:0
Hs Code.:
DSSTox Substance ID:DTXSID60233150
Nikkaji Number:J68.039G
Wikidata:Q83114515
Mol file:84227-74-7.mol

Synonyms:BRN 5982977;84227-74-7;Benzamide, p-amino-N-(o-((diethylamino)methyl)benzyl)-;N,N-Diethyl-2-(p-aminobenzamidomethyl)benzylamine;p-Amino-N-(o-((diethylamino)methyl)benzyl)benzamide;Benzamide, 4-amino-N-((2-((diethylamino)methyl)phenyl)methyl)-;p-Amino-N-[o-[(diethylamino)methyl]benzyl]benzamide;DTXSID60233150;LS-25502

Suppliers and Price of Benzamide, p-amino-N-(o-((diethylamino)methyl)benzyl)-

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 3 raw suppliers

Chemical Property of Benzamide, p-amino-N-(o-((diethylamino)methyl)benzyl)-

Chemical Property:

Vapor Pressure:2.42E-10mmHg at 25°C
Boiling Point:505.5°C at 760 mmHg
Flash Point:259.5°C
PSA：58.36000
Density:1.102g/cm³
LogP:4.01270
XLogP3:2.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:7
Exact Mass:311.199762429
Heavy Atom Count:23
Complexity:349

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCN(CC)CC1=CC=CC=C1CNC(=O)C2=CC=C(C=C2)N

Technology Process of Benzamide, p-amino-N-(o-((diethylamino)methyl)benzyl)-

There total 3 articles about Benzamide, p-amino-N-(o-((diethylamino)methyl)benzyl)- 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: 80.0%

: 84227-71-4
N,N-Diethyl-2-(p-nitrobenzamidomethyl)-benzylamine

: 84227-74-7
N,N-Diethyl 2-(p-aminobenzamidomethyl)-benzylamine

Guidance literature:: With hydrogenchloride; iron; In ethanol; for 3h; Heating;
DOI:10.1002/ardp.19823151205

Reference yield:

: 122-04-3
4-nitro-benzoyl chloride

: 84227-74-7
N,N-Diethyl 2-(p-aminobenzamidomethyl)-benzylamine

Guidance literature:: Multi-step reaction with 2 steps

1: 60 percent / K₂CO₃ / benzene / 3 h / Heating

2: 80 percent / Fe, aq. HCl / ethanol / 3 h / Heating

With hydrogenchloride; iron; potassium carbonate; In ethanol; benzene;
DOI:10.1002/ardp.19823151205

Reference yield:

: 84227-68-9
N-(2-(aminomethyl)benzyl)-N-ethylethylamine

: 84227-74-7
N,N-Diethyl 2-(p-aminobenzamidomethyl)-benzylamine

Guidance literature:: Multi-step reaction with 2 steps

1: 60 percent / K₂CO₃ / benzene / 3 h / Heating

2: 80 percent / Fe, aq. HCl / ethanol / 3 h / Heating

With hydrogenchloride; iron; potassium carbonate; In ethanol; benzene;
DOI:10.1002/ardp.19823151205