N-(4-dodecylphenyl)acetamide

Base Information

Chemical Name:N-(4-dodecylphenyl)acetamide
CAS No.:3663-30-7
Molecular Formula:C20H33 N O
Molecular Weight:303.488
Hs Code.:
NSC Number:172877
DSSTox Substance ID:DTXSID20305948
Wikidata:Q82052779
Mol file:3663-30-7.mol

Synonyms:N-(4-dodecylphenyl)acetamide;3663-30-7;NSC172877;N-Acetyl-4-n-dodecylaniline;SCHEMBL6746649;DTXSID20305948;UJFNBKYAAHOUMD-UHFFFAOYSA-N;STK366286;AKOS005443094;NSC-172877;NCGC00341698-01;AB01333988-02

Suppliers and Price of N-(4-dodecylphenyl)acetamide

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 7 raw suppliers

Chemical Property of N-(4-dodecylphenyl)acetamide

Chemical Property:

Vapor Pressure:1.91E-08mmHg at 25°C
Boiling Point:454.4°Cat760mmHg
Flash Point:281.3°C
Density:0.947g/cm³
XLogP3:7.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:12
Exact Mass:303.256214676
Heavy Atom Count:22
Complexity:269

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCCCCCCC1=CC=C(C=C1)NC(=O)C

Technology Process of N-(4-dodecylphenyl)acetamide

There total 7 articles about N-(4-dodecylphenyl)acetamide 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: 95.0%

: 6313-88-8
4-dodecylacetophenone

: 3663-30-7
N-acetyl-4-n-dodecylaniline

Guidance literature:: With sodium azide; sulfuric acid; In acetic acid; at 60 - 70 ℃; for 5h;

Reference yield: 12.0%

: 592-41-6,25067-06-5
1-hexene

: 622-50-4
4-Acetamido-1-iodobenzene

: 20330-59-0
N-(4-hexylphenyl)acetamide

: 20330-65-8
N-(4-heptylphenyl)acetamide

: 37593-11-6
N-(4-octylphenyl)acetamide

: 37593-12-7
N-(4-nonylphenyl)acetamide

: 37593-13-8
N-(4-decylphenyl)acetamide

: 3663-20-5
N-(4-butylphenyl)acetamide

: 20330-52-3
N-(4-pentylphenyl)acetamide

: 102707-88-0
N-(4-undecylphenyl)acetamide

: 3663-30-7
N-acetyl-4-n-dodecylaniline

: 68777-64-0
N-(4-tridecylphenyl)acetamide

: 72755-62-5
N-(4-tetradecylphenyl)acetamide

Guidance literature:: 1-hexene; With tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; at 70 ℃; for 12h; Inert atmosphere; Sealed tube;

With Schwartz's reagent; In tetrahydrofuran; at 50 ℃; for 5h; Inert atmosphere; Sealed tube;

4-Acetamido-1-iodobenzene; With 4,4'-di-tert-butyl-2,2'-bipyridine nickel(II) bromide; tetrabutylammonium p-toluenesulfonate; In tetrahydrofuran; at 20 ℃; for 24h; Inert atmosphere; Irradiation; Sealed tube;
DOI:10.1016/j.chempr.2019.12.010

Reference yield:

: 4292-19-7
1-Iodododecane

: 3663-30-7
N-acetyl-4-n-dodecylaniline

Guidance literature:: Multi-step reaction with 3 steps

2: cobalt (II)-chloride / 247 °C

With cobalt(II) chloride;
DOI:10.1039/jr9370001119