2-nitrobenzyl benzohydroxamate

Base Information

Chemical Name:2-nitrobenzyl benzohydroxamate
CAS No.:36663-91-9
Molecular Formula:C₁₄H₁₂N₂O₄
Molecular Weight:272.26
Hs Code.:

Synonyms:2-nitrobenzyl benzohydroxamate

Suppliers and Price of 2-nitrobenzyl benzohydroxamate

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

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Chemical Property of 2-nitrobenzyl benzohydroxamate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 2-nitrobenzyl benzohydroxamate

There total 3 articles about 2-nitrobenzyl benzohydroxamate 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: 28.7%

: 495-18-1
Benzohydroxamic acid

: 3958-60-9
2-nitrophenylmethyl bromide

: 36663-91-9
2-nitrobenzyl benzohydroxamate

Guidance literature:: With potassium hydroxide; In ethanol; water; for 4.5h; Reflux;
DOI:10.1016/j.jphotochem.2011.10.005

Reference yield:

: 3958-60-9
2-nitrophenylmethyl bromide

: 36663-91-9
2-nitrobenzyl benzohydroxamate

Guidance literature:: Benzohydroxamic acid; With sodium hydroxide; In water;

2-nitrophenylmethyl bromide; In ethanol; water; for 2h; Heating / reflux;

Reference yield:

: 93-89-0,99341-95-4
benzoic acid ethyl ester

: 36663-91-9
2-nitrobenzyl benzohydroxamate

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / KOH; hydroxylamine hydrochloride / pyridine / 6 h / 20 °C

2: KOH / ethanol; H₂O / 0.75 h / Heating

With potassium hydroxide; hydroxylamine hydrochloride; In pyridine; ethanol; water; 1: Condensation / 2: Alkylation;
DOI:10.1016/S0968-0896(99)00090-5