Basic information Uses Safety Supplier Related

5,7-DIMETHOXY-INDAN-1-ONE

Basic information Uses Safety Supplier Related

5,7-DIMETHOXY-INDAN-1-ONE Basic information

Product Name:
5,7-DIMETHOXY-INDAN-1-ONE
Synonyms:
  • 5,7-DIMETHOXY-INDAN-1-ONE
  • 5,7-Dimethoxy-1-indanone
  • 5,7-diMethoxy-2,3-dihydro-1H-inden-1-one
  • 5,7-dimethoxy-2,3-dihydroinden-1-one
  • 2,3-Dihydro-5,7-dimethoxy-1H-inden-1-one
  • 1H-Inden-1-one, 2,3-dihydro-5,7-dimethoxy-
CAS:
880-87-5
MF:
C11H12O3
MW:
192.21
Mol File:
880-87-5.mol
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5,7-DIMETHOXY-INDAN-1-ONE Chemical Properties

Melting point:
99-100 °C
Boiling point:
352.6±42.0 °C(Predicted)
Density 
1.34 g/cm3
storage temp. 
Sealed in dry,Room Temperature
Appearance
Off-white to light yellow Solid
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5,7-DIMETHOXY-INDAN-1-ONE Usage And Synthesis

Uses

5,7-Dimethoxyindan-1-one acts as a reagent for the preparation and antitumor activities of phenyl- and benzothiazolylisoquinolinedienes.

Uses

5,7-Dimethoxyindan-1-one acts as a reagent for the preparation and antitumor activities of phenyl- and benzothiazolylisoquinolinedienes.

Synthesis

717-94-2

880-87-5

The general procedure for the synthesis of 5,7-dimethoxyindanone from 3,5-dimethoxyphenylpropionic acid was as follows: 3-(3,5-dimethoxyphenyl)propionic acid (2 g x 5) was dissolved in methanesulfonic acid (10 ml x 5) in a microwave treated vial (20 ml x 5). The reaction mixture was heated at 90°C for 10 min under microwave radiation. After completion of the reaction, the mixture was slowly poured into ice (250 g) and neutralized to pH 8-9 with 2 M NaOH solution, followed by extraction with EtOAc. The organic layers were combined and the target product 5,7-dimethoxyindanone (8.8 g, 96.2% yield) was obtained after concentration. The product was analyzed by LC-MS and showed m/e 193 (MH+).

References

[1] Chemistry - An Asian Journal, 2015, vol. 10, # 4, p. 1050 - 1064
[2] Tetrahedron, 2007, vol. 63, # 2, p. 389 - 395
[3] Patent: WO2007/71348, 2007, A1. Location in patent: Page/Page column 87
[4] ChemMedChem, 2018, vol. 13, # 18, p. 1949 - 1956
[5] Tetrahedron Letters, 1980, vol. 21, # 37, p. 3603 - 3606

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