Pentanamide, N-(1-(1-oxo-2-propylpentyl)-4-piperidinyl)-2-propyl-

Base Information

Chemical Name:Pentanamide, N-(1-(1-oxo-2-propylpentyl)-4-piperidinyl)-2-propyl-
CAS No.:128960-25-8
Molecular Formula:C₂₁H₄₀N₂O₂
Molecular Weight:352.561
Hs Code.:
DSSTox Substance ID:DTXSID20156013
Wikidata:Q83024008

Synonyms:BRN 3621734;Pentanamide, N-(1-(1-oxo-2-propylpentyl)-4-piperidinyl)-2-propyl-;N-(1-(2-Propylpentanoyl)-4-piperidinyl)-2-propylpentanamide;N-(1-(1-Oxo-2-propylpentyl)-4-piperidinyl)-2-propylpentanamide;128960-25-8;DTXSID20156013;AKOS005066449;LS-101521

Suppliers and Price of Pentanamide, N-(1-(1-oxo-2-propylpentyl)-4-piperidinyl)-2-propyl-

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 0 raw suppliers

Chemical Property of Pentanamide, N-(1-(1-oxo-2-propylpentyl)-4-piperidinyl)-2-propyl-

Chemical Property:

Vapor Pressure:3.86E-11mmHg at 25°C
Boiling Point:525.6°C at 760 mmHg
Flash Point:271.7°C
Density:0.96g/cm³
XLogP3:5.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:11
Exact Mass:352.308978523
Heavy Atom Count:25
Complexity:377

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCC(CCC)C(=O)NC1CCN(CC1)C(=O)C(CCC)CCC

Technology Process of Pentanamide, N-(1-(1-oxo-2-propylpentyl)-4-piperidinyl)-2-propyl-

There total 2 articles about Pentanamide, N-(1-(1-oxo-2-propylpentyl)-4-piperidinyl)-2-propyl- 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: 84.0%

: 2936-08-5
valproyl chloride

: 128960-11-2
N-(4-piperidinyl)-2-propylpentanamide

: 128960-25-8
N-(1-(2-propylpentanoyl)-4-piperidinyl)-2-propylpentanamide

Guidance literature:: With potassium carbonate; In acetone; for 4h; Heating;

Reference yield:

: 128960-10-1
N-(1-benzyl-4-piperidinyl)-2-propylpentanamide

: 128960-25-8
N-(1-(2-propylpentanoyl)-4-piperidinyl)-2-propylpentanamide

Guidance literature:: Multi-step reaction with 2 steps

1: H₂ / PtO₂ / ethanol / 760 Torr / Ambient temperature

2: 84 percent / K₂CO₃ / acetone / 4 h / Heating

With hydrogen; potassium carbonate; platinum(IV) oxide; In ethanol; acetone;