ChemicalBook--->CAS DataBase List--->60032-57-7

60032-57-7

60032-57-7 Structure

60032-57-7 Structure
IdentificationBack Directory
[Name]

2-METHYLNICOTINALDEHYDE
[CAS]

60032-57-7
[Synonyms]

2-METHYLNICOTINALDEHYDE
2-Methylpyridine-3-carbox...
2-Methylpyridine-3-carbaldehyde
2-Methylpyridine-3-carboxaldehyde
2-Methyl-3-Pyridinecarboxaldehyde
3-Pyridinecarboxaldehyde, 2-Methyl-
2-METHYLNICOTINALDEHYDE ISO 9001:2015 REACH
[Molecular Formula]

C7H7NO
[MDL Number]

MFCD08234911
[MOL File]

60032-57-7.mol
[Molecular Weight]

121.14
Questions And AnswerBack Directory
[Uses]

2-Methylnicotinaldehyde is a useful research chemical.
Chemical PropertiesBack Directory
[Melting point ]

242 °C (decomp)
[Boiling point ]

94 °C(Press: 12 Torr)
[density ]

1.106 g/mL at 25 °C
[refractive index ]

n20/D1.549
[Fp ]

93℃
[storage temp. ]

2-8°C, stored under nitrogen
[form ]

liquid
[pka]

4.15±0.10(Predicted)
[color ]

Pale yellow
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22-37/38-41
[Safety Statements ]

26-39
[WGK Germany ]

3
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

2-METHYLNICOTINALDEHYDE(60032-57-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

(2-METHYL-PYRIDIN-3-YL)-METHANOL

56826-61-0

2-METHYLNICOTINALDEHYDE

60032-57-7

General procedure for the synthesis of 2-methylpyridine-3-carbaldehyde from 2-methylpyridine-3-methanol: A mixture of 3-hydroxymethyl-2-methylpyridine (9.0 g, 73.1 mmol) and manganese(IV) dioxide (28.1 g, 322 mmol) in dichloromethane (100 mL) was heated and refluxed for 48 hours. Upon completion of the reaction, the insoluble material was removed by diatomaceous earth filtration and the filter cake was washed with a solvent mixture of methanol/dichloromethane. Subsequently, the solvent in the filtrate was removed by rotary evaporator to give 2-methylpyridine-3-carboxaldehyde (7.5 g, 85% yield) as an oily product. Its nuclear magnetic resonance hydrogen spectrum (NMR) data were as follows: δ 2.78 (s, 3H), 7.43 (dd, 1H), 8.15 (dd, 1H), 8.66 (dd, 1H).

[References]

[1] Patent: WO2006/106307, 2006, A1. Location in patent: Page/Page column 91
[2] Patent: WO2006/100461, 2006, A1. Location in patent: Page/Page column 83
[3] Chemical and Pharmaceutical Bulletin, 1994, vol. 42, # 9, p. 1841 - 1849
[4] Patent: WO2013/19682, 2013, A1. Location in patent: Page/Page column 101
[5] Patent: WO2013/19626, 2013, A1. Location in patent: Page/Page column 27
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