Benzamide, N,N-bis(3-aminopropyl)-

Base Information

Chemical Name:Benzamide, N,N-bis(3-aminopropyl)-
CAS No.:1652-93-3
Molecular Formula:C₁₃H₂₁N₃O
Molecular Weight:235.329
Hs Code.:
DSSTox Substance ID:DTXSID30441785
Wikidata:Q82258724
Mol file:1652-93-3.mol

Synonyms:Benzamide, N,N-bis(3-aminopropyl)-;1652-93-3;DTXSID30441785

Suppliers and Price of Benzamide, N,N-bis(3-aminopropyl)-

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 2 raw suppliers

Chemical Property of Benzamide, N,N-bis(3-aminopropyl)-

Chemical Property:

XLogP3:-0.7
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:7
Exact Mass:235.168462302
Heavy Atom Count:17
Complexity:207

Purity/Quality:: 99.90% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=O)N(CCCN)CCCN

Technology Process of Benzamide, N,N-bis(3-aminopropyl)-

There total 3 articles about Benzamide, N,N-bis(3-aminopropyl)- 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:

: 1380423-35-7
N,N-bis(3-((E)-2-hydroxybenzylideneamino)propyl)benzamide

: 1652-93-3
N,N-bis(3-aminopropyl)benzamide

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 2h;
DOI:10.1016/j.tetlet.2012.04.070

Reference yield:

: 56-18-8
bis(3-aminopropyl)amine

: 1652-93-3
N,N-bis(3-aminopropyl)benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: methanol / 20 °C / Inert atmosphere

2: triethylamine / ethanol / 20 °C

3: trifluoroacetic acid / dichloromethane / 2 h / 20 °C

With triethylamine; trifluoroacetic acid; In methanol; ethanol; dichloromethane;
DOI:10.1016/j.tetlet.2012.04.070

Reference yield:

: 52279-45-5
2,2′-((1E,1′E)-((azanediylbis(propane-3,1-diyl))bis-(azanylylidene))-bis(methanylylidene))-diphenol

: 1652-93-3
N,N-bis(3-aminopropyl)benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / ethanol / 20 °C

2: trifluoroacetic acid / dichloromethane / 2 h / 20 °C

With triethylamine; trifluoroacetic acid; In ethanol; dichloromethane;
DOI:10.1016/j.tetlet.2012.04.070