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5-Chloro-2-hydroxy-3-nitropyridine

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5-Chloro-2-hydroxy-3-nitropyridine Basic information

Product Name:
5-Chloro-2-hydroxy-3-nitropyridine
Synonyms:
  • 5-CHLORO-2-HYDROXY-3-NITROPYRIDINE
  • 5-CHLORO-3-NITROPYRIDIN-2-OL
  • 5-CHLORO-3-NITRO-2-PYRIDINOL
  • 2-hydroxy-3-nitro-5-chloropyridine
  • 5-Chloro-3-nitropyridin-2-ol, 95+%
  • 5-Chloro-2-hydroxy-3-nitropyridine 95+%
  • 5-Chloro-2-hydroxy-3-nitropyridine ,97%
  • 2-Hydroxy-5-chloro-3-nitropyridine
CAS:
21427-61-2
MF:
C5H3ClN2O3
MW:
174.54
EINECS:
622-609-6
Product Categories:
  • Heterocycle-Pyridine series
  • Chloropyridines
  • Halopyridines
  • Bases & Related Reagents
  • Nucleotides
  • blocks
  • NitroCompounds
  • Pyridines
  • Pyridine
Mol File:
21427-61-2.mol
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5-Chloro-2-hydroxy-3-nitropyridine Chemical Properties

Melting point:
232-236 °C
Boiling point:
284.1±40.0 °C(Predicted)
Density 
1.61±0.1 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
solubility 
soluble in Dimethylformamide
form 
powder to crystal
pka
6.31±0.10(Predicted)
color 
Light yellow to Yellow to Green
BRN 
383852
CAS DataBase Reference
21427-61-2(CAS DataBase Reference)
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Safety Information

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

MSDS

  • Language:English Provider:ALFA
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5-Chloro-2-hydroxy-3-nitropyridine Usage And Synthesis

Chemical Properties

White to light brown solid

Uses

5-Chloro-2-hydroxy-3-nitropyridine (cas# 21427-61-2) is a compound useful in organic synthesis.

Synthesis

1072-98-6

21427-61-2

Preparation of Example A2 5-chloro-2-hydroxy-3-nitropyridine (STR9): 321 g of 2-amino-5-chloropyridine was slowly added dropwise to 1.25 L of concentrated sulfuric acid with continuous stirring until the raw material was completely dissolved. Subsequently, 172.5 g of sodium nitrite (dissolved in 240 mL of water) was slowly added at 40°C to 45°C and the reaction mixture continued to be stirred for 15 minutes. Next, 125 mL of pure nitric acid was slowly added dropwise over 40 minutes at 50°C. The reaction mixture was maintained at 55°C for 1 hour and then the reaction was quenched by pouring into 5 kg of ice water. The yellow precipitated product was collected by filtration, washed thoroughly with deionized water and dried at 60°C to afford 351 g of 5-chloro-2-hydroxy-3-nitropyridine in 80.5% of the theoretical yield and a melting point of 229°C to 231°C.

References

[1] Patent: US5274100, 1993, A
[2] Yakugaku Zasshi, 1952, vol. 72, p. 431
[3] Chem.Abstr., 1953, p. 6404

5-Chloro-2-hydroxy-3-nitropyridine Preparation Products And Raw materials

Raw materials

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