1-Piperidinepropanamide, N-(4-acetylphenyl)-

Base Information

Chemical Name:1-Piperidinepropanamide, N-(4-acetylphenyl)-
CAS No.:90279-42-8
Molecular Formula:C₁₆H₂₂N₂O₂
Molecular Weight:274.363
Hs Code.:
DSSTox Substance ID:DTXSID00399729
Wikidata:Q82202434

Synonyms:1-Piperidinepropanamide, N-(4-acetylphenyl)-;90279-42-8;DTXSID00399729;FCXCFPPWHHRQCD-UHFFFAOYSA-N;AKOS001305622;1-Pyridinepropanamide, N-(4-acetylphenyl)hexahydro-;N-(4-ACETYL-PHENYL)-3-PIPERIDIN-1-YL-PROPIONAMIDE

Suppliers and Price of 1-Piperidinepropanamide, N-(4-acetylphenyl)-

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
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price

Total 0 raw suppliers

Chemical Property of 1-Piperidinepropanamide, N-(4-acetylphenyl)-

Chemical Property:

PSA：49.41000
LogP:2.71460
XLogP3:1.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:274.168127949
Heavy Atom Count:20
Complexity:329

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)C1=CC=C(C=C1)NC(=O)CCN2CCCCC2

Technology Process of 1-Piperidinepropanamide, N-(4-acetylphenyl)-

There total 4 articles about 1-Piperidinepropanamide, N-(4-acetylphenyl)- 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:

: 26371-07-3
1-piperidinepropionic acid

: 90279-42-8
3-piperidino-propionic acid-(4-acetyl-anilide)

Guidance literature:: Multi-step reaction with 2 steps

1: oxalyl chloride / benzene / 0.5 h

2: diethyl ether / 0.08 h

With oxalyl dichloride; In diethyl ether; benzene;