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5-Bromo-3-nitro-2-pyridinol

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5-Bromo-3-nitro-2-pyridinol Basic information

Product Name:
5-Bromo-3-nitro-2-pyridinol
Synonyms:
  • BUTTPARK 43\57-80
  • B217
  • JR-6756, 5-Bromo-3-nitropyridin-2-ol, 97%
  • 5-Bromo-2-hydroxy-3-nitropyridine 97%
  • 5-BROMO-2-HYDROXY-3-NITROPYRIDINE
  • 5-BROMO-3-NITRO-2-PYRIDINOL
  • 5-BROMO-3-NITRO-2(1H)-PYRIDINONE
  • 5-BROMO-3-NITROPYRIDIN-2-OL
CAS:
15862-34-7
MF:
C5H3BrN2O3
MW:
218.99
EINECS:
239-989-0
Product Categories:
  • Nucleotides and Nucleosides
  • Bromopyridines
  • Halopyridines
  • Bases & Related Reagents
  • Nucleotides
  • blocks
  • Bromides
  • NitroCompounds
  • Pyridines
  • Pyridine
  • Pyridine series
Mol File:
15862-34-7.mol
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5-Bromo-3-nitro-2-pyridinol Chemical Properties

Melting point:
246-250 °C
Boiling point:
296.7±40.0 °C(Predicted)
Density 
1.98±0.1 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
solubility 
DMSO, Methanol
pka
6.31±0.10(Predicted)
form 
Solid
color 
Yellow
BRN 
383853
InChI
InChI=1S/C5H3BrN2O3/c6-3-1-4(8(10)11)5(9)7-2-3/h1-2H,(H,7,9)
InChIKey
WXRLCVUDLFFTFF-UHFFFAOYSA-N
SMILES
C1(=O)NC=C(Br)C=C1[N+]([O-])=O
CAS DataBase Reference
15862-34-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xn,Xi
Risk Statements 
22-37/38-41-36/37/38-20
Safety Statements 
26-36/37/39-36
RIDADR 
2811
WGK Germany 
3
Hazard Note 
Harmful
HazardClass 
IRRITANT
HS Code 
29337900

MSDS

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5-Bromo-3-nitro-2-pyridinol Usage And Synthesis

Chemical Properties

Yellow Solid

Uses

5-Bromo-3-nitropyridin-2(1H)-one is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

Synthesis

6945-68-2

15862-34-7

GENERAL METHOD: 2-amino-3-nitro-5-bromopyridine (0.015 mol) was dissolved in 70% sulfuric acid under cooling in an ice bath. A solution prepared from sodium nitrite (1.24 g) dissolved in water (8 mL) was slowly added dropwise in the range of 0-5°C, keeping the reaction temperature constant. After the dropwise addition, the reaction mixture was allowed to warm up gradually to room temperature and stirred continuously at that temperature for 3 hours. After completion of the reaction, the resulting precipitate was separated by filtration, washed well with deionized water and finally dried under vacuum at 60 °C overnight.

References

[1] Tetrahedron, 2014, vol. 70, # 5, p. 1077 - 1083
[2] Journal of the Chemical Society, 1952, p. 2042,2044
[3] Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1999, vol. 38, # 9, p. 1036 - 1040

5-Bromo-3-nitro-2-pyridinol Preparation Products And Raw materials

Preparation Products

Raw materials

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