Benzamide, N,2-dihydroxy-N-phenyl-

Base Information

Chemical Name:Benzamide, N,2-dihydroxy-N-phenyl-
CAS No.:19393-60-3
Molecular Formula:C13H11NO3
Molecular Weight:229.235
Hs Code.:
DSSTox Substance ID:DTXSID20405694
Nikkaji Number:J1.288.469I
Wikidata:Q82210380

Synonyms:Benzamide, N,2-dihydroxy-N-phenyl-;19393-60-3;DTXSID20405694;AKOS004117611

Suppliers and Price of Benzamide, N,2-dihydroxy-N-phenyl-

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 Benzamide, N,2-dihydroxy-N-phenyl-

Chemical Property:

XLogP3:2.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:229.07389321
Heavy Atom Count:17
Complexity:263

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)N(C(=O)C2=CC=CC=C2O)O

Technology Process of Benzamide, N,2-dihydroxy-N-phenyl-

There total 3 articles about Benzamide, N,2-dihydroxy-N-phenyl- 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:

: 22755-09-5
N-phenyl hydroxylamine hydrochloride

: 5538-51-2
O-acetylsalicyloyl chloride

: 19393-60-3
N-phenyl-salicylohydroxamic acid

Guidance literature:: With sodium carbonate; In tetrahydrofuran; dichloromethane; at 25 ℃; for 1h;
DOI:10.1016/S0040-4039(00)00164-7

Reference yield:

: 50-78-2,98201-60-6
aspirin

: 19393-60-3
N-phenyl-salicylohydroxamic acid

Guidance literature:: Multi-step reaction with 2 steps

1: (COCl)2 / CH₂Cl₂ / 1 h / 25 °C / Heating

2: Na₂CO₃ / CH₂Cl₂; tetrahydrofuran / 1 h / 25 °C

With oxalyl dichloride; sodium carbonate; In tetrahydrofuran; dichloromethane; 1: Acid chloride formation / 2: Substitution;
DOI:10.1016/S0040-4039(00)00164-7