ChemicalBook--->CAS DataBase List--->131747-68-7

131747-68-7

131747-68-7 Structure

131747-68-7 Structure
IdentificationBack Directory
[Name]

2-Pyridinecarbonitrile,5-formyl-(9CI)
[CAS]

131747-68-7
[Synonyms]

5-ForMylpicolinonitrile
5-forMylpyridin-2-carbonitrile
5-formylpyridine-2-carbonitrile
5-ForMyl-2-pyridinecarbonitrile
6-Cyanopyridine-3-carboxaldehyde
2-Pyridinecarbonitrile, 5-formyl-
2-cyanopyridine-5-carboxyaldehyde
2-Pyridinecarbonitrile,5-formyl-(9CI)
5-ForMyl-2-pyridinecarbonitrile, 95+%
[Molecular Formula]

C7H4N2O
[MDL Number]

MFCD12755972
[MOL File]

131747-68-7.mol
[Molecular Weight]

132.12
Chemical PropertiesBack Directory
[Melting point ]

86-88°C
[Boiling point ]

331.3±27.0 °C(Predicted)
[density ]

1.24±0.1 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[solubility ]

Chloroform, Methanol
[form ]

Solid
[pka]

-2.12±0.10(Predicted)
[color ]

Off-White to Pale Yellow
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319-H335
[Precautionary statements ]

P260-P280-P301+P312
[HS Code ]

2933399990
Hazard InformationBack Directory
[Uses]

6-Cyanopyridine-3-carboxaldehyde, is an intermediate used for the synthesis of pharmaceutical compounds, such as GLPG0634 (C982190), which is used for treatment of rheumatoid arthritis
[Synthesis]

5-[1,3]Dioxolan-2-yl-pyridine-2-carbonitrile

671776-91-3

2-Pyridinecarbonitrile,5-formyl-(9CI)

131747-68-7

Under nitrogen protection, 5-(1,3-dioxolan-2-yl)pyridine-2-carbonitrile (478 mg, 2.71 mmol) was dissolved in THF (5.0 mL) followed by addition of 1 mol/L hydrochloric acid (5.0 mL). The reaction mixture was stirred at room temperature for 16 hours and then continued at 50 °C for 13 hours. Upon completion of the reaction, the reaction mixture was neutralized with saturated aqueous sodium bicarbonate. The product was extracted with ethyl acetate and the organic phase was washed with saturated brine and dried with anhydrous sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure to give 5-formylpyridine-2-carbonitrile (364 mg, 100% yield).

[References]

[1] Patent: US2013/65905, 2013, A1. Location in patent: Paragraph 0182
[2] Patent: WO2004/24700, 2004, A1. Location in patent: Page 35
Spectrum DetailBack Directory
[Spectrum Detail]

2-Pyridinecarbonitrile,5-formyl-(9CI)(131747-68-7)1HNMR
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