ChemicalBook--->CAS DataBase List--->19490-87-0

19490-87-0

19490-87-0 Structure

19490-87-0 Structure
IdentificationBack Directory
[Name]

7-METHOXY-2-METHYLQUINOLINE
[CAS]

19490-87-0
[Synonyms]

7-METHOXY-2-METHYLQUINOLINE
2-Methyl-7-Methoxyquinoline
Quinoline, 7-methoxy-2-methyl-
[EINECS(EC#)]

803-216-0
[Molecular Formula]

C11H11NO
[MDL Number]

MFCD09787870
[MOL File]

19490-87-0.mol
[Molecular Weight]

173.21
Chemical PropertiesBack Directory
[Boiling point ]

286.0±20.0 °C(Predicted)
[density ]

1.102±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

6.15±0.50(Predicted)
[Appearance]

Colorless to light yellow Liquid
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)Exclamation Mark (GHS07)
GHS05,GHS07
[Signal word ]

Danger
[Hazard statements ]

H302-H318
[Precautionary statements ]

P280-P301+P312+P330-P305+P351+P338+P310
[Hazard Codes ]

Xn
[Risk Statements ]

22-41
[Safety Statements ]

26-39
[WGK Germany ]

3
[HS Code ]

2933499090
Spectrum DetailBack Directory
[Spectrum Detail]

7-METHOXY-2-METHYLQUINOLINE(19490-87-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

Ethanol

64-17-5

m-Anisidine

536-90-3

7-METHOXY-2-METHYLQUINOLINE

19490-87-0

General procedure for the synthesis of 2-methyl-7-methoxyquinoline from ethanol and m-aminoanisole: 0.005 mmol (1.1 mg) of transition metal catalyst was accurately weighed and placed in a 10 mL Young reaction tube equipped with a magnetic stirrer. Under oxygen atmosphere, 0.04 mmol of co-catalyst I, 0.08 mmol of co-catalyst II, 0.2 mmol of 3-methoxyaniline and 1 mL of anhydrous ethanol were added sequentially to the reaction tube. The reaction mixture was stirred at 150 °C for 16 hours. After completion of the reaction, the pH of the reaction solution was adjusted to neutral and left to stand for subsequent processing. The target product 2-methyl-7-methoxyquinoline was purified by column chromatography in 88% yield.

[References]

[1] Patent: CN106543078, 2017, A. Location in patent: Paragraph 0089; 0090
[2] Tetrahedron Letters, 2010, vol. 51, # 37, p. 4911 - 4914
[3] Research on Chemical Intermediates, 2012, vol. 38, # 3-5, p. 761 - 773
[4] Journal of Organic Chemistry, 2017, vol. 82, # 6, p. 3284 - 3290
[5] Synthesis and Reactivity in Inorganic, Metal-Organic and Nano-Metal Chemistry, 2013, vol. 43, # 4, p. 500 - 508
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