Benzaldehyde, 2-hydroxy-5-nitro-, oxime

Base Information

Chemical Name:Benzaldehyde, 2-hydroxy-5-nitro-, oxime
CAS No.:1595-15-9
Molecular Formula:C7H6 N2 O4
Molecular Weight:182.136
Hs Code.:2928000090
DSSTox Substance ID:DTXSID1061811
Mol file:1595-15-9.mol

Synonyms:Benzaldehyde, 2-hydroxy-5-nitro-, oxime;2-(hydroxyiminomethyl)-4-nitrophenol;1595-15-9;2-hydroxy-5-nitrobenzaldehyde oxime;Oprea1_492775;Oprea1_723873;5-nitro-2-hydroxy benzaldoxime;DTXSID1061811;DVBKBUGAIYQNOE-UHFFFAOYSA-N;FT-0772388

Suppliers and Price of Benzaldehyde, 2-hydroxy-5-nitro-, oxime

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

Aronis compounds
2-hydroxy-5-nitrobenzaldehydeoxime
10mg
$ 20.00

Aronis compounds
2-hydroxy-5-nitrobenzaldehydeoxime
1mg
$ 12.00

American Custom Chemicals Corporation
2-HYDROXY-5-NITROBENZALDEHYDE OXIME 95.00%
5MG
$ 499.00

Total 9 raw suppliers

Chemical Property of Benzaldehyde, 2-hydroxy-5-nitro-, oxime

Chemical Property:

Vapor Pressure:0.00018mmHg at 25°C
Melting Point:175-178 °C(Solv: ethanol (64-17-5))
Boiling Point:293.6°C at 760 mmHg
PKA:6.00±0.30(Predicted)
Flash Point:131.4°C
PSA：98.64000
Density:1.51g/cm³
LogP:1.63170
XLogP3:1.7
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:1
Exact Mass:182.03275668
Heavy Atom Count:13
Complexity:213

Purity/Quality:

98%min ^*data from raw suppliers

2-hydroxy-5-nitrobenzaldehydeoxime ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of Benzaldehyde, 2-hydroxy-5-nitro-, oxime

There total 3 articles about Benzaldehyde, 2-hydroxy-5-nitro-, oxime 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: 92.0%

: 97-51-8
5-Nitrosalicylaldehyde

: 1595-15-9
2-hydroxy-5-nitro-benzaldehyde oxime

Guidance literature:: With hydroxylamine hydrochloride; In methanol; water; at 20 ℃; for 1h; pH=3.98; regioselective reaction; Catalytic behavior;
DOI:10.1080/24701556.2021.2025098

Reference yield: 75.0%

: 39224-61-8
2-hydroxy-5-nitrobenzyl alcohol

: 1595-15-9
2-hydroxy-5-nitro-benzaldehyde oxime

Guidance literature:: 2-hydroxy-5-nitrobenzyl alcohol; With dihydrogen peroxide; at 20 ℃; for 0.166667h; Green chemistry;

With hydroxylamine hydrochloride; for 7h; Catalytic behavior; Green chemistry;
DOI:10.1016/j.molstruc.2019.03.008