24099-29-4 Usage
Description
6-ISOPENTENYLOXYISOBERGAPTEN, also known as 5-Methoxy-6-[(3-methyl-2-buten-1-yl)oxy]-2H-furo[2,3-h]-1-benzopyran-2-one, is a naturally occurring compound that has been isolated from the roots of Heracleum leskovii. It is a unique chemical entity with potential applications in various industries due to its distinct properties.
Uses
Used in Pharmaceutical Industry:
6-ISOPENTENYLOXYISOBERGAPTEN is used as a bioactive compound for its potential therapeutic effects. The compound's unique structure and properties make it a promising candidate for the development of new drugs and treatments, particularly in the areas of cancer, inflammation, and other diseases.
Used in Cosmetic Industry:
6-ISOPENTENYLOXYISOBERGAPTEN is used as an active ingredient in the cosmetic industry for its potential benefits in skincare and anti-aging products. Its bioactive properties may contribute to improved skin health, reduced inflammation, and enhanced skin regeneration.
Used in Agricultural Industry:
6-ISOPENTENYLOXYISOBERGAPTEN can be used as a natural pesticide or growth regulator in the agricultural industry. Its bioactive properties may help protect crops from pests and diseases, while also promoting healthy plant growth and development.
Used in Flavor and Fragrance Industry:
Due to its unique chemical structure, 6-ISOPENTENYLOXYISOBERGAPTEN may have potential applications in the flavor and fragrance industry. It could be used to create new and distinct scents or flavors for various products, such as perfumes, candles, and food additives.
Used in Research and Development:
6-ISOPENTENYLOXYISOBERGAPTEN is used as a research compound for studying its chemical properties, potential applications, and mechanisms of action. This can lead to a better understanding of its therapeutic potential and the development of new drugs and products based on its unique properties.
Check Digit Verification of cas no
The CAS Registry Mumber 24099-29-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,0,9 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 24099-29:
(7*2)+(6*4)+(5*0)+(4*9)+(3*9)+(2*2)+(1*9)=114
114 % 10 = 4
So 24099-29-4 is a valid CAS Registry Number.
InChI:InChI=1/C17H16O5/c1-10(2)6-8-21-17-15(19-3)11-4-5-13(18)22-14(11)12-7-9-20-16(12)17/h4-7,9H,8H2,1-3H3
24099-29-4Relevant articles and documents
Efficient Synthesis of Furochromone and Furocoumarin Natural Products (Khellin, Pimpinellin, Isophellopterin) by Thermal Rearrangement of 4-Furyl-4-hydroxycyclobutenones
Reed, Michael W.,Moore, Harold W.
, p. 4166 - 4171 (1988)
Diethyl squarate was converted in three steps to a highly functionalized benzofuran 6b, which served as an intermediate in a high yield synthesis of khellinone (9), a versatile precursor to a variety of linear furochromones, including the natural product khellin.The use of dimethyl squarate gave a similar benzofuran intermediate 6a, which was used in the first total syntheses of the furocoumarins pimpinellin (14) and isophellopterin (15).The key benzofuran intermediates were prepared by thermal rearrangement of (trimethylsilyl)ethynyl-substituted 4-furanyl-4-hydroxycyclobutenones 2a,b.The alkynyl moiety of 6b was readily converted to the acetyl group of khellinone by mercury-catalyzed hydrolysis.Alternatively, the TMS protecting group in 6a was removed, and the lithium acetylide was treated with methyl chloroformate.The resulting trimethoxybenzofuran was treated with CAN to generate the quinone.Catalytic hydrogenation gave reduction of the quinone to the hydroquinone and alkyne to the cis-alkene.Simultaneous lactonization gave the desired coumarin 13.Methylation of this at the phenolic site gave pimpinellin (14).The same phenol was prenylated to give isophellopterin (15).Finally, oxidation of the phenol with CAN gave a previously unknown orthoquinone, (16), and angular isomer of psoralenquinone.
