Produktinformation
Name:
4,5-Dimethoxy-1-indanone
Synonyme:
- 1-Indanone, 4,5-dimethoxy-
- 1H-Inden-1-one, 2,3-dihydro-4,5-dimethoxy-
- 2,3-Dihydro-4,5-dimethoxy-1H-inden-1-one
- 4,5-dimethoxy-2,3-dihydro-1H-inden-1-one
- NSC 46649
Beschreibung:
4,5-Dimethoxy-1-indanone is an acidic compound. It is a synthetic intermediate that has been used as a precursor in the synthesis of several natural products with anticancer activity. 4,5-Dimethoxy-1-indanone can be prepared from eugenol by acidolysis and demethylation reactions. The reaction time for this process ranges from 1 to 3 hours at room temperature. The molecule has two hydrogensulfate groups which are responsible for its acidic character. 4,5-Dimethoxy-1-indanone also has anticancer activity, which may be due to its ability to cause cell death through chloride channels. This molecule is not a steroidal compound and does not bind to the androgen receptor or estrogen receptor.
Hinweis:
Unsere Produkte sind nur für Laborzwecke. Für jede andere Verwendung, bitte melden sie sich bei uns.
Marke:
Biosynth
Langzeitlagerung:
Hinweise:
Chemische Eigenschaften
Molekulargewicht:
192.21 g/mol
Formel:
C11H12O3
Reinheit:
Min. 95%
InChl:
InChI=1S/C11H12O3/c1-13-10-6-4-7-8(11(10)14-2)3-5-9(7)12/h4,6H,3,5H2,1-2H3
InChI Key:
InChIKey=XQODIRIVQXQUFN-UHFFFAOYSA-N
SMILES:
COc1ccc2c(c1OC)CCC2=O
MDL:
Schmelzpunkt:
Siedepunkt:
Flammpunkt:
Dichte:
Konzentration:
EINECS:
Merck:
HS-Code:
