N-Hydroxy-2-methoxy-N-phenylbenzamide

Base Information

Chemical Name:N-Hydroxy-2-methoxy-N-phenylbenzamide
CAS No.:34661-16-0
Molecular Formula:C14H13NO3
Molecular Weight:243.262
Hs Code.:
DSSTox Substance ID:DTXSID40536570
Nikkaji Number:J685.013H
Wikidata:Q82411289
Mol file:34661-16-0.mol

Synonyms:N-Hydroxy-2-methoxy-N-phenylbenzamide;34661-16-0;DTXSID40536570;N-phenyl-o-methoxybenzohydroxamic acid

Suppliers and Price of N-Hydroxy-2-methoxy-N-phenylbenzamide

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of N-Hydroxy-2-methoxy-N-phenylbenzamide

Chemical Property:

PSA：49.77000
LogP:2.73120
XLogP3:1.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:243.08954328
Heavy Atom Count:18
Complexity:276

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC=CC=C1C(=O)N(C2=CC=CC=C2)O

Technology Process of N-Hydroxy-2-methoxy-N-phenylbenzamide

There total 3 articles about N-Hydroxy-2-methoxy-N-phenylbenzamide 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: 94.0%

: 100-65-2
N-Phenylhydroxylamine

: 21615-34-9
2-Methoxybenzoyl chloride

: 34661-16-0
N-(2-methoxybenzoyl)-N-phenylhydroxylamine

Guidance literature:: With sodium hydrogencarbonate; In dichloromethane; at 0 ℃; for 4h;
DOI:10.1055/s-1984-30981

Reference yield: 65.0%

: 586-96-9
Nitrosobenzene

: 135-02-4
ortho-anisaldehyde

: 34661-16-0
N-(2-methoxybenzoyl)-N-phenylhydroxylamine

Guidance literature:: With 3-(N-morpholino)propanesulfonic acid; benzaldehyde lyase; thiamine diphosphate; magnesium sulfate; In dichloromethane; at 30 ℃; for 96h; pH=7; buffer; Enzymatic reaction;
DOI:10.1002/adsc.201000735