N-[2-Oxo-1-(piperidin-1-yl)butyl]benzamide

Base Information

Chemical Name:N-[2-Oxo-1-(piperidin-1-yl)butyl]benzamide
CAS No.:65462-74-0
Molecular Formula:C₁₆H₂₂N₂O₂
Molecular Weight:274.363
Hs Code.:
DSSTox Substance ID:DTXSID60505581

Synonyms:65462-74-0;N-[2-Oxo-1-(piperidin-1-yl)butyl]benzamide;DTXSID60505581;1-benzamido-1-piperidino-2-butanone

Suppliers and Price of N-[2-Oxo-1-(piperidin-1-yl)butyl]benzamide

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 1 raw suppliers

Chemical Property of N-[2-Oxo-1-(piperidin-1-yl)butyl]benzamide

Chemical Property:

XLogP3:2.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:274.168127949
Heavy Atom Count:20
Complexity:331

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCC(=O)C(NC(=O)C1=CC=CC=C1)N2CCCCC2

Technology Process of N-[2-Oxo-1-(piperidin-1-yl)butyl]benzamide

There total 4 articles about N-[2-Oxo-1-(piperidin-1-yl)butyl]benzamide 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: 50.0%

: 110-89-4
piperidine

: 65462-72-8
1-benzamido-3-bromo-2-butanone

: 65462-74-0
1-benzamido-1-piperidino-2-butanone

Guidance literature:: at 20 ℃; for 12h;
DOI:10.1007/BF00949233

Reference yield:

: 17136-94-6
1-benzamido-2-butanol

: 65462-74-0
1-benzamido-1-piperidino-2-butanone

Guidance literature:: Multi-step reaction with 2 steps

1: 91 percent / Br₂, LiCl / acetic acid / 36 h / 20 °C

2: 50 percent / 12 h / 20 °C

With bromine; lithium chloride; In acetic acid;
DOI:10.1007/BF00949233

Reference yield:

: 110-89-4
piperidine

: 17136-94-6
1-benzamido-2-butanol

: 65462-74-0
1-benzamido-1-piperidino-2-butanone

Guidance literature:: With sulfuryl dichloride; Yield given. Multistep reaction; 1) CH₂Cl₂, 20 deg C, 2 h; 2) EtOH, 20 deg C, 12 h;
DOI:10.1007/BF00954664