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ChemicalBook--->CAS DataBase List--->53014-84-9

53014-84-9

53014-84-9 Structure

53014-84-9 Structure
IdentificationBack Directory
[Name]

3-FORMYL-6-METHYL-PYRIDINE
[CAS]

53014-84-9
[Synonyms]

5-FORMYL-2-PICOLINE
6-Methylnicotinaldehyde
5-Formyl-2-methylpyridine
3-FORMYL-6-METHYL-PYRIDINE
3-Formyl-6-methyl-pyridine ,97%
6-Methylpyridine-3-carboxaldehyde
6-METHYL-3-PYRIDINECARBOXALDEHYDE
3-Pyridinecarboxaldehyde, 6-methyl-
6-Methylpyridine-3-carboxaldehyde 97%
5-ForMyl-2-picoline/6-Methylnicotinaldehyde
2-Phenyl-[1,2,4]triazolo[1,5-a]pyridin-6-amine
6-Methylpyridine-3-carboxaldehyde, 5-Formyl-2-methylpyridine
[Molecular Formula]

C7H7NO
[MDL Number]

MFCD08272279
[MOL File]

53014-84-9.mol
[Molecular Weight]

121.14
Chemical PropertiesBack Directory
[Boiling point ]

95℃/20mm
[density ]

1.084
[refractive index ]

1.546
[Fp ]

88℃
[storage temp. ]

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

Liquid
[pka]

4.15±0.10(Predicted)
[Sensitive ]

Moisture Sensitive
[InChIKey]

IMWMEIWYPWVABQ-UHFFFAOYSA-N
[CAS DataBase Reference]

53014-84-9
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22-36
[Safety Statements ]

26
[WGK Germany ]

3
[HS Code ]

29333990
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Tetrahydrofuran-->N,N-Dimethylformamide-->n-Butyllithium-->Magnesium-->2-Chloropropane-->2-Bromo-5-methylpyridine
[Preparation Products]

2-Methyl-5-vinylpyridine-->3-Pyridinepropanoicacid,-bta--amino-6-methyl-(9CI)
Spectrum DetailBack Directory
[Spectrum Detail]

3-FORMYL-6-METHYL-PYRIDINE(53014-84-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

To a solution of 5-bromo-2-methylpyridine (151; 10 g, 58.1 mmol) in THF (150 mL) was added n-BuLi (2.5 M, 25.6 mL) at -78 ℃. The reaction mixture was stirred at this temperature for Ih. DMF (1.30 mL) was added,, and the resulting reaction mixture was stirred for 1 h at -78 °C. The addition of aq quenched the reaction. NH4Cl. Upon warming to room temperature, the mixture was extracted with EtOAc. The combined organic layers were dried (Na2SO4) and concentrated under reduced pressure. The resulting residue was purified by chromatography to afford 6-methylnicotinaldehyde 152 (5.0 g, 72percent).
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