3-(4-Benzyl-piperidin-1-yl)-phenylamine

Base Information

Chemical Name:3-(4-Benzyl-piperidin-1-yl)-phenylamine
CAS No.:478403-42-8
Molecular Formula:C18H22N2
Molecular Weight:266.386
Hs Code.:
DSSTox Substance ID:DTXSID901252489

Synonyms:3-(4-Benzyl-piperidin-1-yl)-phenylamine;SCHEMBL6429226;KJYBMODFQBDVAC-UHFFFAOYSA-N;DTXSID901252489;478403-42-8;3-[4-(Phenylmethyl)-1-piperidinyl]benzenamine

Suppliers and Price of 3-(4-Benzyl-piperidin-1-yl)-phenylamine

Supply Marketing:

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

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Chemical Property of 3-(4-Benzyl-piperidin-1-yl)-phenylamine

Chemical Property:

XLogP3:4.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:266.178298710
Heavy Atom Count:20
Complexity:277

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CN(CCC1CC2=CC=CC=C2)C3=CC=CC(=C3)N

Technology Process of 3-(4-Benzyl-piperidin-1-yl)-phenylamine

There total 4 articles about 3-(4-Benzyl-piperidin-1-yl)-phenylamine 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: 100.0%

: 831203-53-3
4-benzyl-1-(3-nitrophenyl)piperidine

: 478403-42-8
3-(4-benzylpiperidin-1-yl)phenylamine

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol; ethyl acetate; at 20 ℃; for 8h; under 2585.74 Torr;
DOI:10.1021/jm050765n

Reference yield: 100.0%

: 478403-42-8
3-(4-benzylpiperidin-1-yl)phenylamine

Guidance literature:

Reference yield:

: 31252-42-3
4-benzylpyperidine

: 478403-42-8
3-(4-benzylpiperidin-1-yl)phenylamine

Guidance literature:: Multi-step reaction with 2 steps

1: 91 percent / K₂CO₃ / dimethylsulfoxide / 24 h / 90 °C

2: 100 percent / H₂ / Pd/C / ethyl acetate; methanol / 8 h / 20 °C / 2585.74 Torr

With hydrogen; potassium carbonate; palladium on activated charcoal; In methanol; dimethyl sulfoxide; ethyl acetate;
DOI:10.1021/jm050765n