89837-72-9 Usage
Uses
Used in Medicinal Chemistry:
(4aR,8aS,9aS)-9a-hydroxy-4,4,7-trimethyl-4a,5,6,8a,9,9a-hexahydronaphtho[2,3-b]furan-2(4H)-one is used as a compound of interest in medicinal chemistry for its potential to be developed into pharmaceutical agents. Its unique structure may offer novel interactions with biological targets, leading to the discovery of new therapeutic agents.
Used in Pharmacology:
In pharmacology, (4aR,8aS,9aS)-9a-hydroxy-4,4,7-trimethyl-4a,5,6,8a,9,9a-hexahydronaphtho[2,3-b]furan-2(4H)-one may be utilized for studying its effects on biological systems. Understanding its interactions with receptors, enzymes, or other cellular components could reveal its potential as a lead compound for drug development.
Used in Organic Synthesis:
(4aR,8aS,9aS)-9a-hydroxy-4,4,7-trimethyl-4a,5,6,8a,9,9a-hexahydronaphtho[2,3-b]furan-2(4H)-one is also used in the field of organic synthesis as a building block or intermediate for the creation of more complex molecules. Its unique structure and functional groups can be leveraged to synthesize a variety of organic compounds with diverse applications.
Used in Chemical Research:
In chemical research, (4aR,8aS,9aS)-9a-hydroxy-4,4,7-trimethyl-4a,5,6,8a,9,9a-hexahydronaphtho[2,3-b]furan-2(4H)-one serves as a subject for studying the synthesis, properties, and reactivity of naphthofuran compounds. This can contribute to the advancement of organic chemistry and the discovery of new synthetic methods.
Check Digit Verification of cas no
The CAS Registry Mumber 89837-72-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,8,3 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 89837-72:
(7*8)+(6*9)+(5*8)+(4*3)+(3*7)+(2*7)+(1*2)=199
199 % 10 = 9
So 89837-72-9 is a valid CAS Registry Number.
89837-72-9Relevant academic research and scientific papers
Regioselective Oxidation of 3-Alkylfurans to 3-Alkyl-4-hydroxybutenolides
Kernan, Michael R.,Faulkner, John D.
, p. 2773 - 2776 (2007/10/02)
3-Alkyl-4-hydroxybutenolides are synthesized in good to high yields by the oxidation of 3-alkylfurans with singlet oxygen, generated from molecular oxygen with a polymer-bound rose bengal catalyst in dichloromethane solution at -78 deg C, in the presence
Metabolites of the Nudibranch Chromodoris funerea and the Singlet Oxygen Oxidation Products of Furodysin and Furodysinin
Carte, Brad,Kernan, Michael R.,Barrabee, Ellen B.,Faulkner, D. John,Matsumoto, Gayle K.,Clardy, Jon
, p. 3528 - 3532 (2007/10/02)
Methanolic extracts of the nudibranch Chromodoris funerea, found in association with sponges of the genus Dysidea, contained 2-(2,4-dibromophenoxy)-3,4,5-tribromophenol (1), a major metabolite of Dysidea herbacea, O-methylfurodysinin lactone (2), and the
