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2,6-Pyridinedicarbonitrile

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2,6-Pyridinedicarbonitrile Basic information

Product Name:
2,6-Pyridinedicarbonitrile
Synonyms:
  • 26DCPY
  • 2,6-DICYANO PYRIDINE
  • pyridine-2,6-dicarbonitrile
  • 2,6-Pyridinedicarbonitrile(6CI,7CI,8CI,9CI)
  • Dipicolinonitrile
  • 2,6-Pyridinedicarbonitrile
  • 6-Pyridinedicarbonitrile
  • 2,6-Pyridinedicarbonitrile 97%
CAS:
2893-33-6
MF:
C7H3N3
MW:
129.12
EINECS:
220-766-1
Product Categories:
  • Pyridine series, pharma.
  • PYRIDINE
  • C7 and C8
  • Heterocyclic Building Blocks
  • Pyridines
  • john's
Mol File:
2893-33-6.mol
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2,6-Pyridinedicarbonitrile Chemical Properties

Melting point:
123-127 °C (lit.)
Boiling point:
290.0±20.0 °C(Predicted)
Density 
1.25±0.1 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
pka
-5.87±0.10(Predicted)
form 
solid
color 
Off-white to light brown
InChI
InChI=1S/C7H3N3/c8-4-6-2-1-3-7(5-9)10-6/h1-3H
InChIKey
XNPMXMIWHVZGMJ-UHFFFAOYSA-N
SMILES
C1(C#N)=NC(C#N)=CC=C1
CAS DataBase Reference
2893-33-6
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Safety Information

Hazard Codes 
Xn
Risk Statements 
20/21/22-36/37/38
Safety Statements 
26-36
WGK Germany 
3
HS Code 
29333990
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2,6-Pyridinedicarbonitrile Usage And Synthesis

Chemical Properties

white to off-white powder

Uses

2,6-Pyridinedicarbonitrile may be used to synthesize bis-tetrazoles and pyridine-based tridentate ligand 2,6-bis(α-aminoisopropyl)pyridine.

General Description

2,6-Pyridinedicarbonitrile is a heterocyclic dinitrile. Its biotransformation by Rhodococcus erythropolis A4 to 6-cyanopyridine-2-carboxamide has been reported.

Synthesis

499-83-2

2893-33-6

The general procedure for the synthesis of 2,6-pyridinedicarbonitrile from pyridine-2,6-dicarboxylic acid was carried out as follows: liquid ammonia (0.5 ml) and acetonitrile (50 ml) were mixed in a cold bath at -40 °C, followed by the addition of pyridine-2,6-dicarboxylic acid (1.67 g). After raising the temperature of the mixture to 0°C, phosphorus pentachloride (4 g) was added in batches. The reaction mixture was stirred at room temperature for 2 hours to ensure complete reaction. After completion of the reaction, the solvent was removed by concentration under reduced pressure. The residue was dissolved with dichloromethane and subsequently washed with saturated sodium bicarbonate solution to neutrality. The organic layer was dried with anhydrous magnesium sulfate and concentrated again. The resulting solid was recrystallized by isopropanol to give white crystals of 2,6-pyridinedicarbonitrile (1.13 g) in 88% yield.

References

[1] Patent: CN105503716, 2016, A. Location in patent: Paragraph 0016
[2] Journal of Organic Chemistry, 2015, vol. 80, # 5, p. 2676 - 2699
[3] Chemical Communications, 2017, vol. 53, # 42, p. 5718 - 5720

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