4-{[Benzyl(methyl)amino]methyl}aniline

Base Information

Chemical Name:4-{[Benzyl(methyl)amino]methyl}aniline
CAS No.:88465-51-4
Molecular Formula:C15H18N2
Molecular Weight:226.321
Hs Code.:
DSSTox Substance ID:DTXSID00530832
Wikidata:Q82402218

Synonyms:88465-51-4;4-{[Benzyl(methyl)amino]methyl}aniline;SCHEMBL3152066;DTXSID00530832;RIQLJIOFWJEUCA-UHFFFAOYSA-N;AKOS000155275;4-(n-benzyl-n-methyl-aminomethyl)-aniline;4-[(n-benzyl-n-methyl-amino)-methyl]-aniline

Suppliers and Price of 4-{[Benzyl(methyl)amino]methyl}aniline

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of 4-{[Benzyl(methyl)amino]methyl}aniline

Chemical Property:

XLogP3:2.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:226.146998583
Heavy Atom Count:17
Complexity:203

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN(CC1=CC=CC=C1)CC2=CC=C(C=C2)N

Technology Process of 4-{[Benzyl(methyl)amino]methyl}aniline

There total 9 articles about 4-{[Benzyl(methyl)amino]methyl}aniline 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: 97.0%

: 88465-67-2
N-benzyl-N-methyl-1-(4-nitrophenyl)methanamine

: 88465-51-4
4-((benzyl(methyl)amino)methyl)aniline

Guidance literature:: With 5%-palladium/activated carbon; hydrogen; In methanol; at 20 ℃;
DOI:10.1016/j.ejmech.2016.05.055

Reference yield:

: 103-67-3
benzyl-methyl-amine

: 88465-51-4
4-((benzyl(methyl)amino)methyl)aniline

Guidance literature:: Multi-step reaction with 2 steps

2: tin (II)-chloride

With tin(ll) chloride;

Reference yield:

: 100-11-8
1-bromomethyl-4-nitro-benzene

: 88465-51-4
4-((benzyl(methyl)amino)methyl)aniline

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / acetonitrile / 12 h / 80 °C

2: 10% Pt/activated carbon; hydrogen / methanol / 6 h / 15514.9 Torr

With 10% Pt/activated carbon; hydrogen; potassium carbonate; In methanol; acetonitrile;
DOI:10.1016/j.bmc.2013.12.066