ACETOHYDROXAMIC ACID, 2-(p-NITROBENZAMIDO)-

Base Information

Chemical Name:ACETOHYDROXAMIC ACID, 2-(p-NITROBENZAMIDO)-
CAS No.:39735-49-4
Molecular Formula:C9H9N3O5
Molecular Weight:239.21
Hs Code.:
DSSTox Substance ID:DTXSID30192821
Nikkaji Number:J86.337H
Wikidata:Q83065481
Mol file:39735-49-4.mol

Synonyms:2-(p-Nitrobenzamido)acetohydroxamic acid;BRN 2291504;ACETOHYDROXAMIC ACID, 2-(p-NITROBENZAMIDO)-;39735-49-4;DTXSID30192821;2-(p-Nitrobenzoylamino)acetohydroxamic acid

Suppliers and Price of ACETOHYDROXAMIC ACID, 2-(p-NITROBENZAMIDO)-

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

American Custom Chemicals Corporation
2-(PARA-NITROBENZAMIDO)ACETOHYDROXAMIC ACID 95.00%
5MG
$ 496.35

Total 3 raw suppliers

Chemical Property of ACETOHYDROXAMIC ACID, 2-(p-NITROBENZAMIDO)-

Chemical Property:

Refractive Index:1.6500 (estimate)
Boiling Point:381.84°C (rough estimate)
PSA：127.74000
Density:1.48g/cm³
LogP:1.58440
XLogP3:-0.1
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:239.05422040
Heavy Atom Count:17
Complexity:306

Purity/Quality:

99% ^*data from raw suppliers

2-(PARA-NITROBENZAMIDO)ACETOHYDROXAMIC ACID 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1C(=O)NCC(=O)NO)[N+](=O)[O-]

Technology Process of ACETOHYDROXAMIC ACID, 2-(p-NITROBENZAMIDO)-

There total 5 articles about ACETOHYDROXAMIC ACID, 2-(p-NITROBENZAMIDO)- 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:

: C₁₇H₁₄N₃O₆Pol

: 39735-49-4
N-Hydroxycarbamoylmethyl-4-nitro-benzamide

Guidance literature:: With hydroxylamine; sodium hydroxide; In water; isopropyl alcohol; for 15h; Inert atmosphere; solid phase reaction;
DOI:10.1016/j.tetlet.2011.10.103

Reference yield:

: 7512-77-8
ethyl 2-(4-nitrobenzamido)acetate

: 39735-49-4
N-Hydroxycarbamoylmethyl-4-nitro-benzamide

Guidance literature:: With potassium hydroxide; hydroxylamine hydrochloride; In methanol; Yield given; Ambient temperature;
DOI:10.1248/cpb.28.2045

Reference yield:

: 122-04-3
4-nitro-benzoyl chloride

: 39735-49-4
N-Hydroxycarbamoylmethyl-4-nitro-benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: K₂CO₃ / H₂O; toluene / -5 - 5 °C

2: NH₂OH*HCl, KOH / methanol / Ambient temperature

With potassium hydroxide; hydroxylamine hydrochloride; potassium carbonate; In methanol; water; toluene;
DOI:10.1248/cpb.28.2045