N-[(4-Acetamidophenoxy)methyl]benzamide

Base Information

Chemical Name:N-[(4-Acetamidophenoxy)methyl]benzamide
CAS No.:82212-43-9
Molecular Formula:C16H16N2O3
Molecular Weight:284.315
Hs Code.:
DSSTox Substance ID:DTXSID50569410
Nikkaji Number:J463.133A
Wikidata:Q82456558

Synonyms:N-[(4-Acetamidophenoxy)methyl]benzamide;82212-43-9;SCHEMBL10919019;DTXSID50569410

Suppliers and Price of N-[(4-Acetamidophenoxy)methyl]benzamide

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 N-[(4-Acetamidophenoxy)methyl]benzamide

Chemical Property:

XLogP3:2.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:284.11609238
Heavy Atom Count:21
Complexity:345

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(=O)NC1=CC=C(C=C1)OCNC(=O)C2=CC=CC=C2

Technology Process of N-[(4-Acetamidophenoxy)methyl]benzamide

There total 5 articles about N-[(4-Acetamidophenoxy)methyl]benzamide 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: 84.16%

: 103-90-2,8055-08-1
4-acetaminophenol

: 78134-74-4
(benzoylaminomethyl)triethylammonium chloride

: 82212-43-9
1-(acetylamino)-4-(benzamidomethoxy)benzene

Guidance literature:: With TEA; In water; at 20 ℃;
DOI:10.1080/00397919908085975

Reference yield:

: 6282-02-6
N-(hydroxymethyl)benzamide

: 82212-43-9
1-(acetylamino)-4-(benzamidomethoxy)benzene

Guidance literature:: Multi-step reaction with 2 steps

1: 45 percent / SOCl₂ / CH₂Cl₂

2: 1) NEt₃ / 1) CH₂Cl₂

With thionyl chloride; triethylamine; In dichloromethane;
DOI:10.1021/jo00032a020

Reference yield:

: 55-21-0,27208-38-4
benzamide

: 82212-43-9
1-(acetylamino)-4-(benzamidomethoxy)benzene

Guidance literature:: Multi-step reaction with 3 steps

1: 57 percent / K₂CO₃ / H₂O / Heating

2: 45 percent / SOCl₂ / CH₂Cl₂

3: 1) NEt₃ / 1) CH₂Cl₂

With thionyl chloride; potassium carbonate; triethylamine; In dichloromethane; water;
DOI:10.1021/jo00032a020