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3-Bromo-2-chloro-5-nitropyridine

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3-Bromo-2-chloro-5-nitropyridine Basic information

Product Name:
3-Bromo-2-chloro-5-nitropyridine
Synonyms:
  • 3-BROMO-2-CHLORO-5-NITROPYRIDINE
  • 2-CHLORO-3-BROMO-5-NITROPYRIDINE
  • 3-Bromo-2-chloro-5-nitropyridine 98%
  • 2-Chloro-5-nitro-3-bromo pyridine
  • NSC 26278
  • 2 - chloro - 3 - broMine - 5 - nitro pyridine
  • 3-Bromo-2-chloro-5-nitropyridine >
  • Pyridine, 3-bromo-2-chloro-5-nitro-
CAS:
5470-17-7
MF:
C5H2BrClN2O2
MW:
237.44
Product Categories:
  • Heterocycle-Pyridine series
  • Boronic Acid
  • blocks
  • Bromides
  • NitroCompounds
  • Pyridines
  • Pyridine
  • Pyridine series
Mol File:
5470-17-7.mol
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3-Bromo-2-chloro-5-nitropyridine Chemical Properties

Melting point:
54-58
Boiling point:
293.8±35.0 °C(Predicted)
Density 
1.936±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
form 
powder to crystal
pka
-4.99±0.10(Predicted)
color 
Light yellow to Brown to Dark green
InChIKey
PTTQIUHVDDBART-UHFFFAOYSA-N
CAS DataBase Reference
5470-17-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,T
Risk Statements 
25-41
Safety Statements 
26-39-45
RIDADR 
2811
WGK Germany 
1
HazardClass 
IRRITANT
PackingGroup 
HS Code 
2933399990
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3-Bromo-2-chloro-5-nitropyridine Usage And Synthesis

Uses

3-Bromo-2-chloro-5-nitropyridine is a raw material for the preparation of other organic substances and can be used as a reagent or intermediate component in organic synthesis.

Synthesis

3-Bromo-2-chloro-5-nitropyridine is synthesised using 3-Bromo-2-hydroxy-5-nitropyridine as raw material by chemical reaction. The specific synthesis steps are as follows:
Second step POCI3 (3 ml) was added at 0°C to the mixture of 3-Bromo-2-hydroxy-5-nitropyridine (7.25 g, 33 mmol) and quinoline (2 ml, 16.5 mmol). This reaction medium was heated at 12000 for 2.5 hours and then, after cooling to room temperature, 20 ml of water were added. The precipitate formed was collected by filtration and dried to give the expected 3-Bromo-2-chloro-5-nitropyridine in the form of a brown solid, in a yield of 95percent (7.5 g).The NMR analyses (1H 400 MHz DMSO-d6) are in accordance with the expected structure.

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