Benzamide, N-(phenoxymethyl)-

Base Information

Chemical Name:Benzamide, N-(phenoxymethyl)-
CAS No.:82212-42-8
Molecular Formula:C14H13NO2
Molecular Weight:227.263
Hs Code.:
DSSTox Substance ID:DTXSID20472886
Nikkaji Number:J463.127G
Wikidata:Q82302075

Synonyms:Benzamide, N-(phenoxymethyl)-;82212-42-8;SCHEMBL3225336;DTXSID20472886

Suppliers and Price of Benzamide, N-(phenoxymethyl)-

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 Benzamide, N-(phenoxymethyl)-

Chemical Property:

XLogP3:3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:227.094628657
Heavy Atom Count:17
Complexity:230

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=O)NCOC2=CC=CC=C2

Technology Process of Benzamide, N-(phenoxymethyl)-

There total 6 articles about Benzamide, N-(phenoxymethyl)- 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: 96.38%

: 78134-74-4
(benzoylaminomethyl)triethylammonium chloride

: 108-95-2,27073-41-2
phenol

: 82212-42-8
benzamidomethyl phenyl ether

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

Reference yield: 29.0%

: 1019770-60-5
BF₄^(1-)*C₂₆H₂₃NOP⁽¹⁺⁾

: 108-95-2,27073-41-2
phenol

: 82212-42-8
benzamidomethyl phenyl ether

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In acetonitrile; at 60 ℃; for 8h; Sealed tube; Microwave irradiation;
DOI:10.1080/10426507.2012.744014

Reference yield:

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

: 82212-42-8
benzamidomethyl phenyl ether

Guidance literature:: Multi-step reaction with 2 steps

1: 45 percent / SOCl₂ / CH₂Cl₂

2: 1) NEt₃ / 1) CH₂Cl₂, 2) 5 h

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