Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Pharmaceutical intermediates >  Heterocyclic compound >  Quinoline compounds >  5,6,7,8-TETRAHYDROQUINOLINONE-5

5,6,7,8-TETRAHYDROQUINOLINONE-5

Basic information Safety Supplier Related

5,6,7,8-TETRAHYDROQUINOLINONE-5 Basic information

Product Name:
5,6,7,8-TETRAHYDROQUINOLINONE-5
Synonyms:
  • 5,6,7,8-TETRAHYDROQUINOLINONE-5
  • 5,6,7,8-TETRAHYDRO-5-QUINOLINONE
  • 7,8-DIHYDRO-6H-QUINOLIN-5-ONE
  • 5,6,7,8-Tetrahydroquinolin-5-one
  • 7,8-Dihydroquinoline-5(6H)-one
  • 7,8-dihydroquinolin-5(6H)-one
  • 5(6H)-Quinolinone, 7,8-dihydro-
  • 7,8-dihydro-5(6H)-Quinoli...
CAS:
53400-41-2
MF:
C9H9NO
MW:
147.17
Product Categories:
  • Quinoline Derivertives
  • pharmacetical
Mol File:
53400-41-2.mol
More
Less

5,6,7,8-TETRAHYDROQUINOLINONE-5 Chemical Properties

Boiling point:
116-117 °C(Press: 6 Torr)
Density 
1.168±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
solubility 
Chloroform (Sparingly), Methanol (Slightly)
pka
3.85±0.20(Predicted)
form 
liquid
color 
Yellow-brown
InChI
InChI=1S/C9H9NO/c11-9-5-1-4-8-7(9)3-2-6-10-8/h2-3,6H,1,4-5H2
InChIKey
YHHBKPWMEXGLKE-UHFFFAOYSA-N
SMILES
N1C2=C(C(=O)CCC2)C=CC=1
More
Less

Safety Information

HS Code 
2933499090
More
Less

5,6,7,8-TETRAHYDROQUINOLINONE-5 Usage And Synthesis

Uses

7,8-Dihydro-5(6H)-quinolone is used as a reagent in the synthesis of pyridino N-alkylated nicotine analogs which can serve as nicotinic acetylcholine receptor antagonists. 7,8-Dihydro-5(6H)-quinolone is also used in the total synthesis of (±)-tangutorine, a novel indole alkaloid.

Synthesis

10500-57-9

53400-41-2

The general procedure for the synthesis of 5,6,7,8-tetrahydroquinolin-5-one from 5,6,7,8-tetrahydroquinoline was as follows: 0.883 mg of Mn(OTf)2 (0.5 mol%), 67 mg of 5,6,7,8-tetrahydroquinoline, 0.35 g of 65% aqueous TBHP and 2.5 mL of water were added sequentially to 25 mL of a round bottomed flask. The reaction mixture was stirred in air at room temperature for 24 hours. Upon completion of the reaction, the reaction solution was extracted with ethyl acetate (3 x 5 mL), the organic phases were combined and dried over anhydrous sodium sulfate. After filtration, the solvent was removed by concentration under reduced pressure. The crude product was purified by silica gel column chromatography using petroleum ether with ethyl acetate (5:1, v/v) as eluent to afford the target compound 5,6,7,8-tetrahydroquinolin-5-one (56.6 mg, 77% yield) as a pale yellow liquid.

References

[1] Patent: CN105669548, 2016, A. Location in patent: Paragraph 0029; 0030

5,6,7,8-TETRAHYDROQUINOLINONE-5Supplier

Shanghai Changer Pharmaceutical Technology Co. Ltd. Gold
Tel
15921595598
Email
qd.yu@pharmachanger.com
Jinan Kabotang Biological Technology Co.,Ltd. Gold
Tel
0531-61320525 15866703830
Email
figo.gao@foxmail.com
J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
BeiJing Hwrk Chemicals Limted
Tel
0757-86329057 18934348241
Email
sales4.gd@hwrkchemical.com
Jia Xing Isenchem Co.,Ltd
Tel
0573-85285100 18627885956
Email
isenchem@163.com