104653-89-6 Usage
Uses
Used in Pharmaceutical Industry:
Fusarochromanone is used as a pharmaceutical candidate for its potential therapeutic properties. Its unique chemical structure allows it to interact with biological targets, making it a promising compound for the development of new drugs.
Used in Research and Development:
Fusarochromanone is used as a research tool in the study of fungal metabolites and their effects on biological systems. It can help scientists understand the mechanisms of action of mycotoxins and their potential applications in medicine and other fields.
Used in Agriculture:
Fusarochromanone can be used as a biocontrol agent in agriculture to protect crops from fungal infections. Its antimicrobial properties can help control the growth of harmful fungi and reduce the need for chemical fungicides.
Used in Environmental Applications:
Fusarochromanone can be used in environmental applications to break down pollutants and contaminants. Its ability to interact with various chemical compounds makes it a potential candidate for bioremediation and environmental cleanup efforts.
Used in Cosmetics Industry:
Fusarochromanone can be used as an ingredient in cosmetics for its potential skin care benefits. Its antimicrobial and anti-inflammatory properties may contribute to improved skin health and appearance.
Check Digit Verification of cas no
The CAS Registry Mumber 104653-89-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,6,5 and 3 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 104653-89:
(8*1)+(7*0)+(6*4)+(5*6)+(4*5)+(3*3)+(2*8)+(1*9)=116
116 % 10 = 6
So 104653-89-6 is a valid CAS Registry Number.
InChI:InChI=1/C15H20N2O4/c1-15(2)6-11(20)13-12(21-15)4-3-9(14(13)17)10(19)5-8(16)7-18/h3-4,8,18H,5-7,16-17H2,1-2H3
104653-89-6Relevant academic research and scientific papers
Concise synthesis of fungal metabolite (+)-fusarochromanone via rhodium(III)-catalyzed oxidative sp2 C-H bond olefination
Takahama, Yuji,Shibata, Yu,Tanaka, Ken
supporting information, p. 1177 - 1179 (2016/10/18)
The concise synthesis of a fungal metabolite, (+)-fusarochromanone (FC-101), was achieved via the oxidative sp2 C-H bond olefination of an N-acetylaminochromanone with a chiral functionalized electron-rich alkene, catalyzed by an electron-deficient (η5-cyclopentadienyl)rhodium(III) complex, [CpERhCl2]2, under ambient conditions as the key step. This protocol was applied to various acetanilides and functionalized electron-rich alkenes for the syntheses of fusarochromanone analogs.
SYNTHESIS OF CHROMANONES
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Page 46, (2008/06/13)
Processes for the preparation of biologically active chromanones are disclosed, including processes for the preparation of intermediates useful in the preparation of the biologically active chromanones. The chromanones and the intermediates disclosed herein may be useful for a variety of therapies, including the treatment of various cancers and the treatment of inflammation and inflammation related disorders.
