N-(4-methoxyphenyl)heptanamide

Base Information

Chemical Name:N-(4-methoxyphenyl)heptanamide
CAS No.:512173-24-9
Molecular Formula:C14H21NO2
Molecular Weight:235.326
Hs Code.:
DSSTox Substance ID:DTXSID40391409
Nikkaji Number:J1.887.950F
Wikidata:Q82188860
Mol file:512173-24-9.mol

Synonyms:N-(4-methoxyphenyl)heptanamide;Heptanamide, N-(4-methoxyphenyl)-;512173-24-9;SCHEMBL12215287;DTXSID40391409;AKOS003887682

Suppliers and Price of N-(4-methoxyphenyl)heptanamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of N-(4-methoxyphenyl)heptanamide

Chemical Property:

XLogP3:3.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:7
Exact Mass:235.157228913
Heavy Atom Count:17
Complexity:210

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCCCCC(=O)NC1=CC=C(C=C1)OC

Technology Process of N-(4-methoxyphenyl)heptanamide

There total 7 articles about N-(4-methoxyphenyl)heptanamide 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%

: 111-14-8
oenanthic acid

: 104-94-9
4-methoxy-aniline

: 512173-24-9
heptanoic acid (4-methoxyphenyl)-amide

Guidance literature:: With aluminum oxide; In neat (no solvent); at 140 ℃; for 3h; Green chemistry;
DOI:10.1039/c2gc35880h

Reference yield:

: 55917-07-2
heptanoic acid benzylamide

: 51-66-1
4-methoxyacetanilide

: 588-46-5
N-(phenylmethyl)acetamide

: 512173-24-9
heptanoic acid (4-methoxyphenyl)-amide

Guidance literature:: With N-acetyl-N-benzylacetamide; potassium hydride; In diethylene glycol dimethyl ether; at 120 ℃; for 18h;
DOI:10.1002/anie.200603588