56252-06-3 Usage
Uses
Used in Pharmaceutical Industry:
1H-Phenalen-1-one, 2-methoxy-9-(4-methoxyphenyl)is utilized as a pharmaceutical candidate for its potential medicinal applications, leveraging its unique structure and properties to target specific biological processes or conditions. The exact application reasons and mechanisms of action are yet to be determined through ongoing research and development.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 1H-Phenalen-1-one, 2-methoxy-9-(4-methoxyphenyl)serves as a subject of study for its potential to contribute to the discovery of new drugs or therapeutic agents. Its chemical properties and interactions with biological systems are under investigation to understand its full potential in treating diseases or improving health outcomes.
Check Digit Verification of cas no
The CAS Registry Mumber 56252-06-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,2,5 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 56252-06:
(7*5)+(6*6)+(5*2)+(4*5)+(3*2)+(2*0)+(1*6)=113
113 % 10 = 3
So 56252-06-3 is a valid CAS Registry Number.
56252-06-3Relevant articles and documents
Phenylphenalenone-type Phytoalexins from Unripe Bungulan Banana Fruit
Kamo, Tsunashi,Kato, Nagomi,Hirai, Nobuhiro,Tsuda, Mitsuya,Fujioka, Daie,Ohigashi, Hajime
, p. 95 - 101 (1998)
Fourteen phenylphenalenone-type phytoalexins (1-14), including three new compounds, were isolated from the peel of unripe Musa acuminata [AAA] cv. Bungulan fruit which had been injured and then inoculated with conidia of Colletotrichum musae. These new phytoalexins were identified as (+)-cis-2,3-dihydro-2,3-dihydroxy-4-(4′-hydroxyphenyl)phenalen-1-one (12), 9-(3′,4′-dimethoxyphenyl)-2-methoxyphenalen-1-one (13) and 9-(4′-hydroxyphenyl)-2-methoxyphenalen-1-one (14). The ratios of the relative intensities of the [M]+/[M-H]+ ions or [M-H2O]+ /[M-H2O-H]+ ions in the EI mass spectra were applied to discriminate between 4- and 9-phenylphenalenones. An antifungal test on the phytoalexins showed that a phenolic hydroxyl group was essential for the activity.
