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4-Methoxypyridine N-oxide

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4-Methoxypyridine N-oxide Basic information

Product Name:
4-Methoxypyridine N-oxide
Synonyms:
  • AKOS 93569
  • p-methoxypyridine n-oxide
  • 4-Methoxypyridine 1-oxide
  • 4-METHOXYPYRIDINE 1-OXIDE HYDRATE
  • 4-METHOXYPYRIDINE N-OXIDE
  • 4-METHOXYPYRIDINE-N-OXIDE 95%
  • 4-Methoxy-1-oxidopyridin-1-ium
  • Pyridine,4-methoxy-,1-oxide
CAS:
1122-96-9
MF:
C6H7NO2
MW:
125.13
EINECS:
214-367-1
Product Categories:
  • Heterocycle-Pyridine series
  • Pyridines, Pyrimidines, Purines and Pteredines
  • Pyridine
  • Pyridines
  • Aromatics
  • Catalyst
  • Heterocycles
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
Mol File:
1122-96-9.mol
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4-Methoxypyridine N-oxide Chemical Properties

Melting point:
73-79 °C
Boiling point:
308.9±15.0 °C(Predicted)
Density 
1.09±0.1 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
pka
2.30±0.10(Predicted)
form 
powder to crystal
color 
White to Yellow to Orange
Sensitive 
Hygroscopic
λmax
282nm(CH3CN)(lit.)
BRN 
115212
InChI
InChI=1S/C6H7NO2/c1-9-6-2-4-7(8)5-3-6/h2-5H,1H3
InChIKey
BOFAIBPJCWFJFT-UHFFFAOYSA-N
SMILES
C1[N+]([O-])=CC=C(OC)C=1
CAS DataBase Reference
1122-96-9(CAS DataBase Reference)
NIST Chemistry Reference
Pyridine, 4-methoxy-1-oxide-(1122-96-9)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-37/39-24/25-37
WGK Germany 
3
3-10
HS Code 
29333990

MSDS

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4-Methoxypyridine N-oxide Usage And Synthesis

Chemical Properties

Orange Solid

Uses

4-Methoxypyridine N-oxide is a heteroaromatic N-oxide used as a nucleophilic catalyst in oligonucleotide synthesis and free radical polymerization.

Synthesis

In a 25-mL round-bottomed two-necked flask, 4 mL of methanol was added, followed by 4-methoxypyridine (0.5 mmol, 54.6 mg), 30% H2O2 (6.0 eq., 0.3 mL), potassium carbonate (4.0 eq., 276.4 mg), and SO2F2 gas was introduced into the gas stream by using two straight pistons with straight bends and a hose to connect a balloon on one side. The reaction was carried out under sealed conditions with stirring for 20-40 min at room temperature of 23-32 ??C. After the reaction, the potassium carbonate solid was removed by filtration, dried with anhydrous sodium sulfate to remove water and filtered again, and the solvent was concentrated to obtain the crude product, which was finally isolated and purified by column chromatography to give 40.3 mg of 4-methoxypyridinium nitride in a yield of 65.4%.

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