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2-Methyl-5-nitropyridine

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CAS:21203-68-9
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2-Methyl-5-nitropyridine manufacturers

  • 2-Methyl-5-nitropyridine
  • 2-Methyl-5-nitropyridine pictures
  • $5.00 / 1KG
  • 2024-04-08
  • CAS:21203-68-9
  • Min. Order: 1KG
  • Purity: 98%
  • Supply Ability: g-kg-tons, free sample is available
  • 5-Nitro-2-picoline
  • 5-Nitro-2-picoline pictures
  • $0.00 / 25kg
  • 2024-03-28
  • CAS:21203-68-9
  • Min. Order: 25kg
  • Purity: 98%
  • Supply Ability: Inquiry
  • 2-Methyl-5-nitropyridine
  • 2-Methyl-5-nitropyridine pictures
  • $0.00 / 1Kg/Bag
  • 2021-09-29
  • CAS:21203-68-9
  • Min. Order: 1KG
  • Purity: 98%min HPLC
  • Supply Ability: 100KGS
2-Methyl-5-nitropyridine Basic information
Product Name:2-Methyl-5-nitropyridine
Synonyms:Pyridine, 2-methyl-5-nitro- (9CI);2-METHYL-5-NITROPYRIDINE;5-NITRO-2-PICOLINE;AURORA KA-6797;2-METHYL-5-NITROPYRIDINE, 95+%;2-METHYL-5-NITROPYRIDINE/5-NITRO-2-PICOLINE;2-Methyl-5-nitropyridine Hydrochloride;21203-68-9 2-Methyl-5-nitropyridine
CAS:21203-68-9
MF:C6H6N2O2
MW:138.12
EINECS:677-568-7
Product Categories:blocks;Pyridine;Pyridines, Pyrimidines, Purines and Pteredines;NITRO;pyridines
Mol File:21203-68-9.mol
2-Methyl-5-nitropyridine Structure
2-Methyl-5-nitropyridine Chemical Properties
Melting point 112 C
Boiling point 237.1±20.0 °C(Predicted)
density 1.246±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Room Temperature
pka1.92±0.10(Predicted)
form Solid
color Light yellow to Brown
Water Solubility Slightly soluble in water.
InChIInChI=1S/C6H6N2O2/c1-5-2-3-6(4-7-5)8(9)10/h2-4H,1H3
InChIKeyUSZINSZJSVMICC-UHFFFAOYSA-N
SMILESC1(C)=NC=C([N+]([O-])=O)C=C1
CAS DataBase Reference21203-68-9(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
HS Code 2933399990
MSDS Information
2-Methyl-5-nitropyridine Usage And Synthesis
Uses2-Methyl-5-nitropyridine is used as pharmaceutical intermediate.
Synthesis2-(5-nitro-pyridin-2-yl)-malonic acid diethyl ester could be used as a starting material to synthesize 2-methyl-5-nitropyridine. The specific operations are as follows: To 2-(5-nitro-pyridin-2-yl)-malonic acid diethyl ester (12.0 g, 42.5 mmol) was added cold aq. 20% sulfuric acid (120 mL) and the mixture was heated to 100 ℃ for 2h. The cooled reaction was added to a cold dilute sodium hydroxide solution and the pH adjusted to 10. The organics were extracted with dichloromethane (x 4), and then the combined organic phases were dried over sodium sulfate. The filtrate was concentrated to afford 2-methyl-5-nitropyridine (5.0 g, 83 %) as a brown solid. 2-Methyl-5-nitropyridine
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