3-Ethyl-4-nitropyridine 1-oxide

Base Information

Chemical Name:3-Ethyl-4-nitropyridine 1-oxide
CAS No.:35363-12-3
Molecular Formula:C₇H₈N₂O₃
Molecular Weight:168.152
Hs Code.:2933399090
DSSTox Substance ID:DTXSID40188851
Wikidata:Q83060705
Mol file:35363-12-3.mol

Synonyms:3-Ethyl-4-nitropyridine 1-oxide;35363-12-3;Pyridine, 3-ethyl-4-nitro-, 1-oxide;3-ethyl-4-nitro-1-oxidopyridin-1-ium;3-ETHYL-4-NITROPYRIDINE-1-OXIDE;3-ethyl-4-nitropyridin-1-ium-1-olate;BRN 0151134;4-20-00-02761 (Beilstein Handbook Reference);SCHEMBL3341806;3-Ethyl-4-nitropyridine1-oxide;4-nitro-3-ethylpyridine N-oxide;DTXSID40188851;AKOS006275228;CS-0232128;EN300-126354;AC-907/25004687

Suppliers and Price of 3-Ethyl-4-nitropyridine 1-oxide

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

TRC
3-ethyl-4-nitropyridin-1-ium-1-olate
25mg
$ 65.00

American Custom Chemicals Corporation
3-ETHYL-4-NITROPYRIDINE-1-OXIDE 95.00%
5MG
$ 504.80

Total 11 raw suppliers

Chemical Property of 3-Ethyl-4-nitropyridine 1-oxide

Chemical Property:

Vapor Pressure:2.26E-05mmHg at 25°C
Refractive Index:1.5200 (estimate)
Boiling Point:371.1°C at 760 mmHg
PKA:-1.22±0.10(Predicted)
Flash Point:178.2°C
PSA：71.28000
Density:1.3g/cm³
LogP:2.10890
XLogP3:0.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:168.05349212
Heavy Atom Count:12
Complexity:169

Purity/Quality:

98%,99%, ^*data from raw suppliers

3-ethyl-4-nitropyridin-1-ium-1-olate ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCC1=C(C=C[N+](=C1)[O-])[N+](=O)[O-]

Technology Process of 3-Ethyl-4-nitropyridine 1-oxide

There total 2 articles about 3-Ethyl-4-nitropyridine 1-oxide 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:

: 14906-62-8
3-ethylpyridine N-oxide

: 35363-12-3
3-ethyl-4-nitropyridine N-oxide

Guidance literature:: With sulfuric acid; nitric acid;

Reference yield:

: 35363-12-3
3-ethyl-4-nitropyridine N-oxide

Guidance literature:: 3-Aethyl-pyridin-1-oxid u. HNO3 (D=1,50) + H2SO4 (D=1,84) bei 90-100grad;
DOI:10.1039/jr9600004953

Reference yield:

: 35363-12-3
3-ethyl-4-nitropyridine N-oxide

: 76139-74-7
N-(3-ethyl-1-oxido-4-pyridyl)-2-acetyl-3,5-dimethylphenol-4-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: H₂ / 10 percent Pd-C / H₂O; ethanol / Ambient temperature

2: Et₃N / CHCl₃ / -5 - 0 °C

With hydrogen; palladium on activated charcoal; triethylamine; In ethanol; chloroform; water;