Basic information Safety Supplier Related

6-NITROIMIDAZO[1,2-A]PYRIDINE

Basic information Safety Supplier Related

6-NITROIMIDAZO[1,2-A]PYRIDINE Basic information

Product Name:
6-NITROIMIDAZO[1,2-A]PYRIDINE
Synonyms:
  • 6-NITROIMIDAZO[1,2-A]PYRIDINE
  • IMidazo[1,2-a]pyridine, 6-nitro-
  • 6-nitrosoimidazo[1,2-a]pyridine
CAS:
25045-82-3
MF:
C7H5N3O2
MW:
163.13
Mol File:
25045-82-3.mol
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6-NITROIMIDAZO[1,2-A]PYRIDINE Chemical Properties

Melting point:
229-231°
Density 
1.49±0.1 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
3.70±0.50(Predicted)
Appearance
Yellow to brown Solid
InChI
InChI=1S/C7H5N3O2/c11-10(12)6-1-2-7-8-3-4-9(7)5-6/h1-5H
InChIKey
RXZZQEFTZIHXRI-UHFFFAOYSA-N
SMILES
C12=NC=CN1C=C([N+]([O-])=O)C=C2
CAS DataBase Reference
25045-82-3
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Safety Information

HazardClass 
IRRITANT
HS Code 
2933399990
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6-NITROIMIDAZO[1,2-A]PYRIDINE Usage And Synthesis

Synthesis

4214-76-0

2032-35-1

25045-82-3

In a 250 mL single-neck flask, bromoacetaldehyde diethyl acetal (42.5 g, 215.7 mmol) was dissolved in a mixture of 1 mol/L hydrochloric acid (120 mL) and ethanol (20 mL) and stirred at room temperature for 30 minutes. It was then heated to reflux and stirred continuously until the solution became clear. Upon completion of the reaction, the solution was cooled to room temperature and the pH was adjusted to near neutral with sodium bicarbonate solution. 2-Amino-5-nitropyridine (15.0 g, 107.8 mmol) was added and the reaction was stirred overnight at room temperature. At the end of the reaction, extraction was carried out with ethyl acetate (100 mL×3), the organic phases were combined, and the solvent was removed by concentration under reduced pressure. The crude product was purified by silica gel column chromatography (eluent ratio: petroleum ether:ethyl acetate = 2:1) to afford 13.7 g of yellow-brown crystalline 6-nitroimidazo[1,2-a]pyridine in 77.6% yield.

References

[1] Patent: CN107129496, 2017, A. Location in patent: Paragraph 0026-0028; 0014-0016; 0020-0022

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