N-benzylpiperidine-1-carboxamide

Base Information

Chemical Name:N-benzylpiperidine-1-carboxamide
CAS No.:39531-35-6
Molecular Formula:C13H18N2O
Molecular Weight:218.299
Hs Code.:
DSSTox Substance ID:DTXSID30388121
Nikkaji Number:J1.286.391H
Wikidata:Q82182867

Synonyms:N-benzylpiperidine-1-carboxamide;39531-35-6;1-Piperidinecarboxamide, N-(phenylmethyl)-;F3083-0401;SCHEMBL5217325;DTXSID30388121;HMS1602C20;STK257509;AKOS002244852;SR-01000302613;SR-01000302613-1;Z123605672

Suppliers and Price of N-benzylpiperidine-1-carboxamide

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
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Total 0 raw suppliers

Chemical Property of N-benzylpiperidine-1-carboxamide

Chemical Property:

XLogP3:1.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:218.141913202
Heavy Atom Count:16
Complexity:218

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CCN(CC1)C(=O)NCC2=CC=CC=C2

Technology Process of N-benzylpiperidine-1-carboxamide

There total 25 articles about N-benzylpiperidine-1-carboxamide 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%

: 110-89-4
piperidine

: 3173-56-6
benzyl isothiocyanate

: 39531-35-6
N-benzyl-N',N'-(1,5-pentamethylenediyl)urea

Guidance literature:: for 3h;
DOI:10.1039/b315426b

Reference yield: 95.0%

: 110-89-4
piperidine

: 39896-97-4
benzyl-carbamic acid benzyl ester

: 39531-35-6
N-benzyl-N',N'-(1,5-pentamethylenediyl)urea

Guidance literature:: With trimethylaluminum; In toluene; at 50 ℃; for 4.5h;
DOI:10.1016/j.tet.2004.02.034

Reference yield: 94.0%

: 17738-04-4
piperidine-1-carboxylic acid allyl ester

: 100-46-9
benzylamine

: 39531-35-6
N-benzyl-N',N'-(1,5-pentamethylenediyl)urea

Guidance literature:: benzylamine; With bis(trimethylaluminum)–1,4-diazabicyclo[2.2.2]octane adduct; In toluene; at 40 ℃; for 0.333333h;

piperidine-1-carboxylic acid allyl ester; In toluene; at 90 ℃; for 2h;
DOI:10.1016/j.tet.2018.06.011