| Identification | More | [Name]
2-FORMYL-4-PICOLINE | [CAS]
53547-60-7 | [Synonyms]
2-FORMYL-4-PICOLINE
4-METHYLPYRIDINE-2-CARBOXALDEHYDE
4-Methylpyridine-2-carboxaldehyde 95%
2-FORMYL-4-METHYLPYRIDINE
4-Methylpicolinaldehyde | [Molecular Formula]
C7H7NO | [MDL Number]
MFCD07367933 | [Molecular Weight]
121.14 | [MOL File]
53547-60-7.mol |
| Chemical Properties | Back Directory | [Boiling point ]
94-97 °C(Press: 15 Torr) | [density ]
1.082 g/mL at 25 °C | [refractive index ]
n20/D1.531 | [Fp ]
85℃ | [storage temp. ]
under inert gas (nitrogen or Argon) at 2-8°C | [form ]
liquid | [pka]
4.54±0.10(Predicted) | [color ]
Clear, light yellow | [InChI]
1S/C7H7NO/c1-6-2-3-8-7(4-6)5-9/h2-5H,1H3 | [InChIKey]
UAKMHSRHDUBNJR-UHFFFAOYSA-N | [SMILES]
Cc1ccnc(C=O)c1 | [CAS DataBase Reference]
53547-60-7(CAS DataBase Reference) |
| Safety Data | Back Directory | [Symbol(GHS) ]
GHS07 | [Signal word ]
Warning | [Hazard statements ]
H302-H319 | [Precautionary statements ]
P305+P351+P338 | [Hazard Codes ]
Xi | [Risk Statements ]
22 | [WGK Germany ]
3 | [Hazard Note ]
Harmful | [HS Code ]
2933399990 | [Storage Class]
10 - Combustible liquids | [Hazard Classifications]
Acute Tox. 4 Oral
Eye Irrit. 2 |
| Hazard Information | Back Directory | [Synthesis]
The general procedure for the synthesis of 4-methyl-2-pyridinecarboxaldehyde from 2-cyano-4-methylpyridine and the compound (CAS:102854-88-6) is as follows: with reference to Example 55, a toluene solution of diisobutylaluminum hydride (1.5 M, 43.5 mL, 65 mmol) was added slowly and dropwise to 2-cyano-4-methylpyridine (7.0 g, 59 mmol) in a dichloromethane solution (180 mL). The reaction mixture was kept stirred at -78 °C for 2 hours. Subsequently, concentrated hydrochloric acid (28 mL) and water (112 mL) were added to the reaction mixture and the aqueous and organic layers were combined. After separating the organic layer, the organic layer was extracted with 2 N hydrochloric acid. All aqueous layers were combined, neutralized with sodium bicarbonate solution, and extracted with ether. The extracts were sequentially washed with saturated brine and dried with anhydrous magnesium sulfate. Finally, the solvent was removed by evaporation to afford the target product 4-methyl-2-pyridinecarboxaldehyde (2.7 g, 37% yield). | [References]
[1] Patent: EP1424336, 2004, A1. Location in patent: Page 139 |
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