Benzamide, N-[(4-methoxyphenyl)methoxy]-

Base Information

Chemical Name:Benzamide, N-[(4-methoxyphenyl)methoxy]-
CAS No.:92851-07-5
Molecular Formula:C15H15NO3
Molecular Weight:257.289
Hs Code.:
DSSTox Substance ID:DTXSID20438982
Nikkaji Number:J1.838.386A
Wikidata:Q82254841

Synonyms:Benzamide, N-[(4-methoxyphenyl)methoxy]-;92851-07-5;DTXSID20438982;N-(4-Methoxyphenyl)methoxybenzamide

Suppliers and Price of Benzamide, N-[(4-methoxyphenyl)methoxy]-

Supply Marketing:

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

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Chemical Property of Benzamide, N-[(4-methoxyphenyl)methoxy]-

Chemical Property:

XLogP3:2.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:257.10519334
Heavy Atom Count:19
Complexity:269

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC=C(C=C1)CONC(=O)C2=CC=CC=C2

Technology Process of Benzamide, N-[(4-methoxyphenyl)methoxy]-

There total 3 articles about Benzamide, N-[(4-methoxyphenyl)methoxy]- 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: 75.0%

: 7007-15-0
3-benzoyl-1,3-oxazolidin-2-one

: 21038-22-2
O-(4-methoxybenzyl)hydroxylamine

: 92851-07-5
p-methoxybenzyl benzohydroxamate

Guidance literature:: With samarium(III) trifluoromethanesulfonate; In tetrahydrofuran; at 20 ℃; for 1h;
DOI:10.1021/ol0263301

Reference yield: 19.0%

: 495-18-1
Benzohydroxamic acid

: 824-94-2
p-methoxybenzyl chloride

: 92851-07-5
p-methoxybenzyl benzohydroxamate

Guidance literature:: With triethylamine; In chloroform; for 2h; Heating;

Reference yield:

: 105-13-5
4-Methoxybenzyl alcohol

: 92851-07-5
p-methoxybenzyl benzohydroxamate

Guidance literature:: Multi-step reaction with 2 steps

1: HCl-H₂SO₄ / diethyl ether / Heating

2: 19 percent / triethylamine / CHCl₃ / 2 h / Heating

With hydrogenchloride; sulfuric acid; triethylamine; In diethyl ether; chloroform;