57959-88-3 Usage
Description
3,12-Dihydro-6,11-dihydroxy-3,3-dimethyl-7H-pyrano[2,3-c]acridin-7-one is an acridone alkaloid that has been isolated from Atalantia macrophylla. Its structure has been confirmed through spectroscopic evidence and chemical reactions, featuring a unique arrangement of methyl, hydroxyl, and pyrano groups within its molecular framework.
Uses
Used in Pharmaceutical Industry:
3,12-Dihydro-6,11-dihydroxy-3,3-dimethyl-7H-pyrano[2,3-c]acridin-7-one is used as a pharmaceutical compound for its potential therapeutic applications. The presence of multiple functional groups in its structure suggests that it may interact with various biological targets, making it a candidate for the development of new drugs.
Used in Chemical Research:
In the field of chemical research, 3,12-Dihydro-6,11-dihydroxy-3,3-dimethyl-7H-pyrano[2,3-c]acridin-7-one serves as a valuable compound for studying the properties and reactivity of acridone alkaloids. Its unique structure can provide insights into the synthesis and modification of similar compounds, potentially leading to the discovery of new molecules with diverse applications.
Used in Natural Product Analysis:
3,12-Dihydro-6,11-dihydroxy-3,3-dimethyl-7H-pyrano[2,3-c]acridin-7-one is used in the analysis of natural products derived from plants, such as Atalantia macrophylla. Its identification and characterization contribute to the understanding of the chemical diversity and potential bioactive properties of compounds found in nature.
References
Basa, Experientia, 31,1387 (1975)
Check Digit Verification of cas no
The CAS Registry Mumber 57959-88-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,9,5 and 9 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 57959-88:
(7*5)+(6*7)+(5*9)+(4*5)+(3*9)+(2*8)+(1*8)=193
193 % 10 = 3
So 57959-88-3 is a valid CAS Registry Number.
57959-88-3Relevant articles and documents
Synthesis of Acridone Alkaloids: Glycocitrine-I, N-Methylatalphylline, Atalphyllidine, 11-Hydroxyacronycine and 11-Hydroxynoracronycine
Ramesh, Kakarla,Kapil, R. S.
, p. 684 - 687 (2007/10/02)
Selective benzylation of 1,3,5-trihydroxyacridone (3) results in 5-benzylated acridone (6), which on prenylation affords a mixture of monoprenylated acridone (7) and diprenylated acridone (9).Treatment of 7 with methyl iodide followed by hydrogenolysis furnishes glycocitrine-I (1). 9 on benzylation, followed by N-methylation and debenzylation yields N-methylatalphylline (2).Condensation of 6 with 3-hydroxyisovaleraldehyde dimethylacetal results in 15, which on hydrogenolysis furnishes atalphyllidine (12). 15 on methylation affords N-methylacridone (16) and N,O-dimethylacridone (17).Compounds 16 and 17 on hydrogenolysis afford 11-hydroxynoracronycine (13) and 11-hydroxyacronycine (14), respectively.
