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ChemicalBook--->CAS DataBase List--->1849-53-2

1849-53-2

1849-53-2 Structure

1849-53-2 Structure
IdentificationBack Directory
[Name]

3-METHOXY-PYRIDINE-2-CARBALDEHYDE
[CAS]

1849-53-2
[Synonyms]

3-Methoxypicolinaldehyde
3-METHOXY-PYRIDINECARBOXALDEHYDE
3-METHOXY-PYRIDINE-2-CARBALDEHYDE
3-METHOXY-2-PYRIDINECARBOXALDEHYDE
3-Methoxypyridine-2-carboxaldehyde
2-Pyridinecarboxaldehyde, 3-methoxy-
3-Methoxy-2-pyridinecarboxaldehyde ,97%
[Molecular Formula]

C7H7NO2
[MDL Number]

MFCD05664031
[MOL File]

1849-53-2.mol
[Molecular Weight]

137.14
Chemical PropertiesBack Directory
[Melting point ]

67-68 °C
[Boiling point ]

239.4±20.0 °C(Predicted)
[density ]

1.159±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Store in freezer, under -20°C
[form ]

solid
[pka]

3.19±0.10(Predicted)
[Appearance]

Light yellow to green yellow Solid
[InChI]

InChI=1S/C7H7NO2/c1-10-7-3-2-4-8-6(7)5-9/h2-5H,1H3
[InChIKey]

GHKILJGWQPBQGL-UHFFFAOYSA-N
[SMILES]

C1(C=O)=NC=CC=C1OC
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22-37/38-41
[Safety Statements ]

26-39
[HS Code ]

2933399990
Raw materials And Preparation ProductsBack Directory
[Raw materials]

3-methoxy-2-methylpyridine-->Selenium dioxide-->1,4-Dioxane
Hazard InformationBack Directory
[Uses]

3-Methoxypyridine-2-carbaldehyde is a useful reactant and reagent for organic reactions and synthesis.
[Synthesis Reference(s)]

Tetrahedron Letters, 29, p. 773, 1988 DOI: 10.1016/S0040-4039(00)80206-3
[Synthesis]

3-methoxy-2-methylpyridine

26395-26-6

3-METHOXY-PYRIDINE-2-CARBALDEHYDE

1849-53-2

General procedure for the synthesis of 3-methoxypyridine-2-carbaldehyde using 3-methoxy-2-methylpyridine as starting material: selenium dioxide (478 mg, 4.30 mmol) was dissolved in dioxane (8 mL) and heated to 80 °C. Subsequently, a solution of 3-methoxy-2-methylpyridine (265 mg, 2.15 mmol) in dioxane (2 mL) was slowly added. The reaction mixture was continuously stirred at 80 °C for 18 hours. After completion of the reaction, the mixture was cooled to room temperature and filtered to remove insoluble impurities. The filtrate was concentrated under reduced pressure to remove the solvent to give the crude product. Finally, the crude product was purified by column chromatography to afford the target compound 3-methoxypyridine-2-carboxaldehyde as a yellow gel in 27% yield.

[References]

[1] Patent: CN103570683, 2018, B. Location in patent: Paragraph 0748; 0753; 0757; 0758
Spectrum DetailBack Directory
[Spectrum Detail]

3-METHOXY-PYRIDINE-2-CARBALDEHYDE(1849-53-2)1HNMR
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