484-74-2 Usage
Uses
Used in Pharmaceutical Industry:
9-Methylfuro[2,3-b]quinolin-4(9H)-one is used as a pharmaceutical compound for its potential therapeutic applications. Its unique chemical structure and properties make it a candidate for the development of new drugs, particularly in the treatment of various diseases and conditions.
Used in Chemical Research:
In the field of chemical research, 9-Methylfuro[2,3-b]quinolin-4(9H)-one serves as a valuable compound for studying the properties and behavior of quinolone alkaloids. Its hygroscopic nature and light-sensitive characteristics provide insights into the reactivity and stability of similar compounds, contributing to the advancement of chemical knowledge.
Used in Natural Product Extraction:
9-Methylfuro[2,3-b]quinolin-4(9H)-one is used as a marker compound in the extraction and analysis of natural products from plant sources like Dictamnus albus and Helietta longifoliata. Its presence in these plants can help identify and characterize the bioactive components present, which may have potential applications in medicine, agriculture, or other industries.
Used in Material Science:
Due to its light-sensitive properties, 9-Methylfuro[2,3-b]quinolin-4(9H)-one can be utilized in the development of new materials with specific optical or electronic properties. Its ability to change color upon exposure to light may be harnessed for applications in sensors, display technologies, or other optoelectronic devices.
References
Gellert et al., Herb. Hung., 10, 123 (1971)
Mammarella, Comin., An. Asoc. Quim. Argentina, 59, 239 (1971)
Check Digit Verification of cas no
The CAS Registry Mumber 484-74-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,8 and 4 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 484-74:
(5*4)+(4*8)+(3*4)+(2*7)+(1*4)=82
82 % 10 = 2
So 484-74-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H9NO2/c1-13-10-5-3-2-4-8(10)11(14)9-6-7-15-12(9)13/h2-7H,1H3
484-74-2Relevant academic research and scientific papers
Rhodium-Mediated Dipolar Cycloaddition of Diazoquinolinediones
Pirrung, Michael C.,Blume, Florian
, p. 3642 - 3649 (2007/10/03)
As an entry to furoquinoline structures of natural origin, the rhodium-mediated dipolar cycloaddition of diazoquinolinediones with alkenes and alkynes has been examined. Because of the unsymmetrical nature of the diazo compounds, both linear and angular furoquinoline products are possible. For the most part, a mixture of regioisomers is generated in moderate to good yields, though in a few cases dominant products are obtained in high yields. The products can be further converted to naturally occurring alkaloids such as isodictamnine. A novel observation in this work is that catalytic quantities of acid enhance the yield and regiochemical control in the cycloaddition.
