2-Buten-1-one, 1-phenyl-3-(1-piperidinyl)-

Base Information

Chemical Name:2-Buten-1-one, 1-phenyl-3-(1-piperidinyl)-
CAS No.:4620-54-6
Molecular Formula:C15H19NO
Molecular Weight:229.31700
Hs Code.:2933399090
DSSTox Substance ID:DTXSID00346334
Mol file:4620-54-6.mol

Synonyms:4620-54-6;2-Buten-1-one, 1-phenyl-3-(1-piperidinyl)-;Oprea1_835287;DTXSID00346334

Suppliers and Price of 2-Buten-1-one, 1-phenyl-3-(1-piperidinyl)-

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 2-Buten-1-one, 1-phenyl-3-(1-piperidinyl)-

Chemical Property:

PSA：20.31000
LogP:3.19690
XLogP3:3.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:229.146664230
Heavy Atom Count:17
Complexity:283

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=CC(=O)C1=CC=CC=C1)N2CCCCC2

Technology Process of 2-Buten-1-one, 1-phenyl-3-(1-piperidinyl)-

There total 7 articles about 2-Buten-1-one, 1-phenyl-3-(1-piperidinyl)- 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: 61.0%

: 145930-92-3
1-[1-(2-Oxo-2-phenyl-ethylsulfanyl)-ethylidene]-piperidinium; bromide

: 4620-54-6
3-piperidino-1-phenyl-2-buten-1-one

Guidance literature:: With triethylamine; triphenylphosphine; In dichloromethane; for 2h; Ambient temperature;

Reference yield:

: 110-89-4
piperidine

: 93-91-4
1-phenylbutan-1,3-dione

: 4620-54-6
3-piperidino-1-phenyl-2-buten-1-one

Guidance literature:: With hydrogenchloride;
DOI:10.1021/ja01243a002

Reference yield:

: 5309-92-2
1-thioacetyl-piperidine

: 4620-54-6
3-piperidino-1-phenyl-2-buten-1-one

Guidance literature:: Multi-step reaction with 2 steps

1: CH₂Cl₂ / 12 h / Ambient temperature

2: 61 percent / Ph₃P, Et₃N / CH₂Cl₂ / 2 h / Ambient temperature

With triethylamine; triphenylphosphine; In dichloromethane;