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6-Chloro-2-methyl-3-nitropyridine

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6-Chloro-2-methyl-3-nitropyridine Basic information

Product Name:
6-Chloro-2-methyl-3-nitropyridine
Synonyms:
  • TIMTEC-BB SBB003832
  • TIMTEC-BB SBB003830
  • 2-CHLORO-6-METHYL-5-NITROPYRIDINE
  • 2-CHLORO-6-METHYL-3-NITROPYRIDINE
  • 2-CHLORO-5-NITRO-6-METHYLPYRIDINE
  • 2-CHLORO-5-NITRO-6-PICOLINE
  • 6-CHLORO-3-NITRO-2-METHYLPYRIDINE
  • 6-CHLORO-3-NITRO-2-PICOLINE
CAS:
22280-60-0
MF:
C6H5ClN2O2
MW:
172.57
Product Categories:
  • Pyridine
  • compounds of pyridine
  • Boronic Acid
  • Chlorinated heterocyclic series
  • pyridine series
  • Heterocycle-Pyridine series
  • Pyridines
Mol File:
22280-60-0.mol
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6-Chloro-2-methyl-3-nitropyridine Chemical Properties

Melting point:
54-58 °C
Boiling point:
200°C (rough estimate)
Density 
1.5610 (rough estimate)
refractive index 
1.5500 (estimate)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
pka
-3.26±0.10(Predicted)
form 
Powder
color 
Light beige to brown
InChI
InChI=1S/C6H5ClN2O2/c1-4-5(9(10)11)2-3-6(7)8-4/h2-3H,1H3
InChIKey
GHSRMSJVYMITDX-UHFFFAOYSA-N
SMILES
C1(C)=NC(Cl)=CC=C1[N+]([O-])=O
CAS DataBase Reference
22280-60-0(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xn,Xi
Risk Statements 
36/37/38-20/21/22-22
Safety Statements 
36/37/39-26
Hazard Note 
Harmful
HazardClass 
IRRITANT
HS Code 
29333990

MSDS

  • Language:English Provider:ACROS
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6-Chloro-2-methyl-3-nitropyridine Usage And Synthesis

Chemical Properties

Light yellow Cryst

Uses

6-Chloro-2-methyl-3-nitropyridine has been used as a reactant for the synthesis of fluorine-containing pyridinealdoxime derivatives as treatment of organophosphorus nerve-agent poisoning.

Preparation

A mixture of 2-oxo-5-nitro-6-methyl-1,2-dihydropyridine, phosphorous oxychloride, and phosphorous pentachloride was heated at 110° C for 2 hours, whereupon the reaction mixture was charged with an additional portion of phosphorous pentachloride and phosphorous oxychloride. The reaction was stirred for 1 hour and then poured into ice water. The brown solid was filtered and washed with cold water, to give 6-Chloro-2-methyl-3-nitropyridine (94%).

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