Basic information Safety Supplier Related

7-methoxyquinoline

Basic information Safety Supplier Related

7-methoxyquinoline Basic information

Product Name:
7-methoxyquinoline
Synonyms:
  • 7-methoxyquinoline
  • Quinoline, 7-methoxy-
CAS:
4964-76-5
MF:
C10H9NO
MW:
159.18
Product Categories:
  • Chemical Amines
  • Amines
  • Aromatics
Mol File:
4964-76-5.mol
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7-methoxyquinoline Chemical Properties

Boiling point:
143-145 °C(Press: 11 Torr)
Density 
1.130±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
solubility 
Chloroform
form 
Oil
pka
5.26±0.14(Predicted)
color 
Yellow
InChI
InChI=1S/C10H9NO/c1-12-9-5-4-8-3-2-6-11-10(8)7-9/h2-7H,1H3
InChIKey
IVHJSNNMKJWPFW-UHFFFAOYSA-N
SMILES
N1C2C(=CC=C(OC)C=2)C=CC=1
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7-methoxyquinoline Usage And Synthesis

Chemical Properties

Yellow Oil

Uses

7-Methoxyquinoline (cas# 4964-76-5) is a compound useful in organic synthesis.

Synthesis

580-20-1

74-88-4

4964-76-5

General procedure for the synthesis of 7-methoxyquinoline from 7-hydroxyquinoline and iodomethane: 7-hydroxyquinoline (8 g, 55.11 mmol) was added to a solution of sodium hydride (5.5 g, 137.50 mmol, 60% pure) in N,N-dimethylformamide (150 mL). The reaction mixture was stirred in a water/ice bath at 0 °C for 1 hour. Subsequently, iodomethane (7.84 g, 55.23 mmol) was added and the reaction solution was continued to be stirred at room temperature for 1 hour. Upon completion of the reaction, the reaction was quenched by the addition of a water/ice mixture (700 mL) and extracted with ethyl acetate (3 x 200 mL). The organic layers were combined, dried with anhydrous sodium sulfate and concentrated under reduced pressure to give the crude product. The crude product was purified by silica gel column chromatography, using a petroleum ether solution of 6% ethyl acetate as eluent to give 7-methoxyquinoline as a red oil (5.5 g). The product was analyzed by LC-MS showing [M+H]+ peak of 160.0. 1H-NMR (300 MHz, CDCl3) data were as follows: δ 8.84-8.86 (m, 1H), 8.07-8.11 (m, 1H), 7.70-7.73 (t, J = 5.1 Hz, 1H), 7.44 (d, J = 2.4 Hz, 1H). 7.20-7.30 (m, 2H), 3.95 (s, 3H). Case No. BIOE0009-401-PC.

References

[1] Synthetic Communications, 2000, vol. 30, # 2, p. 367 - 375
[2] Patent: WO2012/94462, 2012, A2. Location in patent: Page/Page column 82
[3] Patent: WO2016/86200, 2016, A1. Location in patent: Page/Page column 278
[4] Patent: WO2012/58125, 2012, A1. Location in patent: Page/Page column 115; 116

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