Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Pharmaceutical intermediates >  Heterocyclic compound >  Pyridine compound >  Nitropyridine >  2-Methyl-4-nitropyridine

2-Methyl-4-nitropyridine

Basic information Safety Supplier Related

2-Methyl-4-nitropyridine Basic information

Product Name:
2-Methyl-4-nitropyridine
Synonyms:
  • 2-METHYL-4-NITROPYRIDINE
  • 4-NITRO-2-METHYLPYRIDINE
  • 4-NITRO-2-PICOLINE
  • Pyridine, 2-methyl-4-nitro- (9CI)
  • 2-METHYL-4-NITROPYRIDINE,4-NITRO-2-PICOLINE
  • Pyridine, 2-methyl-4-nitro-
  • 2-Methyl-4-nitropyridine ,97%
  • 2-Mehtyl-4-nitropyridine
CAS:
13508-96-8
MF:
C6H6N2O2
MW:
138.12
EINECS:
640-476-2
Product Categories:
  • Aromatics
  • Bases & Related Reagents
  • Nucleotides
  • Pyridine series
  • Pyridines derivates
  • Building Blocks
  • Aromatics Compounds
  • NITRO
  • blocks
  • NitroCompounds
  • Pyridines
  • Pyridine
Mol File:
13508-96-8.mol
More
Less

2-Methyl-4-nitropyridine Chemical Properties

Melting point:
32-34 °C
Boiling point:
241.5±20.0 °C(Predicted)
Density 
1.246±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
solubility 
Chloroform, Dichloromethane
form 
Solid
pka
2.04±0.10(Predicted)
color 
Yellow
CAS DataBase Reference
13508-96-8(CAS DataBase Reference)
More
Less

Safety Information

Hazard Codes 
Xn
Risk Statements 
22-41
Safety Statements 
26-39-24/25
HS Code 
29333990
More
Less

2-Methyl-4-nitropyridine Usage And Synthesis

Chemical Properties

Yellow Solid

Uses

2-Methyl-4-nitropyridine (cas# 13508-96-8) is a compound useful in organic synthesis.

Synthesis

5470-66-6

13508-96-8

a) To a chloroform solution of 4-nitro-2-methylpyridine-N-oxide (11 g, 71.5 mmol) was slowly added a chloroform solution of phosphorus trichloride (PCl3, 33 mL, 0.37 mmol) at 0 °C and under argon protection. The reaction mixture was stirred at room temperature for 3 hours. Upon completion of the reaction, the mixture was poured into ice water and neutralized with ammonium hydroxide solution to neutral, followed by extraction with dichloromethane. The organic phases were combined and concentrated to give a yellow solid product. The solid was washed with a mixed ether-petroleum ether solvent to give 7.8 g of 2-methyl-4-nitropyridine in 79% yield with a melting point of 35 °C.

References

[1] Organic Letters, 2000, vol. 2, # 22, p. 3525 - 3526
[2] Chemical and Pharmaceutical Bulletin, 1998, vol. 46, # 10, p. 1656 - 1657
[3] Chemical and Pharmaceutical Bulletin, 1990, vol. 38, # 9, p. 2446 - 2458
[4] Journal of Organic Chemistry, 1998, vol. 63, # 15, p. 5013 - 5030
[5] Synlett, 2009, # 18, p. 2927 - 2930

2-Methyl-4-nitropyridine Preparation Products And Raw materials

Preparation Products

Raw materials

2-Methyl-4-nitropyridineSupplier

Shanghai Boyle Chemical Co., Ltd.
Tel
021-50182298 021-50180596
Email
sales@boylechem.com
J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006356688 18621169109
Email
market03@meryer.com
INTATRADE GmbH
Tel
+49 3493/605464
Email
sales@intatrade.de
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com