Nonanamide, N-phenyl-

Base Information

Chemical Name:Nonanamide, N-phenyl-
CAS No.:55679-48-6
Molecular Formula:C15H23NO
Molecular Weight:233.354
Hs Code.:
DSSTox Substance ID:DTXSID30409385
Nikkaji Number:J1.753.260J

Synonyms:Nonanamide, N-phenyl-;55679-48-6;N-phenylnonanamide;Pelargonanilid;SCHEMBL2138777;DTXSID30409385;AKOS003866765

Suppliers and Price of Nonanamide, N-phenyl-

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 Nonanamide, N-phenyl-

Chemical Property:

XLogP3:4.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:8
Exact Mass:233.177964357
Heavy Atom Count:17
Complexity:197

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCCC(=O)NC1=CC=CC=C1

Technology Process of Nonanamide, N-phenyl-

There total 15 articles about Nonanamide, N-phenyl- 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%

: 111-66-0,25068-25-1
oct-1-ene

: 201230-82-2
carbon monoxide

: 62-53-3
aniline

: 55679-48-6
N-phenylnonanamide

Guidance literature:: With palladium(II) acetylacetonate; In toluene; at 100 ℃; for 20h; under 30003 Torr; Solvent; Reagent/catalyst; regioselective reaction; Catalytic behavior; Autoclave; Inert atmosphere;
DOI:10.1002/anie.201308455

Reference yield: 94.0%

: 112-05-0
nonanoic acid

: 62-53-3
aniline

: 55679-48-6
N-phenylnonanamide

Guidance literature:: With pyridine; 2-Chloro-5-methyl-3-phenyl-Δ⁴-1,3,4,2-oxadiazaphospholine; for 4h; Ambient temperature;
DOI:10.1246/bcsj.66.327

Reference yield: 82.0%

: 629-27-6
1-Iodooctane

: 201230-82-2
carbon monoxide

: 98-95-3,26969-40-4
nitrobenzene

: 55679-48-6
N-phenylnonanamide

Guidance literature:: With phenylsilane; C₂₁H₂₃Cl₃CuN₂; sodium hydroxide; In 1,4-dioxane; at 70 ℃; for 30h; Temperature; Catalytic behavior; Glovebox;
DOI:10.1021/acs.orglett.9b04092