ChemicalBook--->CAS DataBase List--->160906-98-9

160906-98-9

160906-98-9 Structure

160906-98-9 Structure
IdentificationBack Directory
[Name]

6-chloro-5-nitronicotinonitrile
[CAS]

160906-98-9
[Synonyms]

6-chloro-5-nitronicotinonitrile
6-CHLORO-5-NITROPYRIDINE-3-CARBONITRILE
3-Pyridinecarbonitrile, 6-chloro-5-nitro-
[Molecular Formula]

C6H2ClN3O2
[MDL Number]

MFCD18905778
[MOL File]

160906-98-9.mol
[Molecular Weight]

183.55
Chemical PropertiesBack Directory
[Boiling point ]

295.9±40.0 °C(Predicted)
[density ]

1.57±0.1 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[pka]

-6.30±0.10(Predicted)
[Appearance]

Light yellow to yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P280-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

6-chloro-5-nitronicotinonitrile(160906-98-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

6-Hydroxy-5-nitronicotinonitrile

320405-84-3

6-chloro-5-nitronicotinonitrile

160906-98-9

GENERAL PROCEDURE: 2-hydroxy-3-nitropyridine (0.015 mol) was suspended in trichlorophosphorus (15 mL). Anhydrous N,N-dimethylformamide (2 mL) was added and the reaction mixture was heated to reflux for 12 hours. Upon completion of the reaction, the excess phosphorous trichloride was removed by distillation. The residue was dissolved in a mixture of dichloromethane and ice and stirred for 30 minutes. The organic layer was separated, washed three times with water, dried over anhydrous sodium sulfate, filtered and concentrated to give analytically pure 6-chloro-5-nitronicotinonitrile.

[References]

[1] Tetrahedron, 2014, vol. 70, # 5, p. 1077 - 1083
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