16981-20-7 Usage
Description
5,7-Dihydroxy-8-(3-methyl-2-butenyl)-6-(2-methylpropanoyl)-4-phenyl-2H-1-benzopyran-2-one is a complex organic compound belonging to the class of flavonoids, specifically a type of flavanone. It is characterized by its unique molecular structure that includes hydroxyl groups, a 3-methyl-2-butenyl group, a 2-methylpropanoyl group, and a phenyl ring. 5,7-Dihydroxy-8-(3-methyl-2-butenyl)-6-(2-methylpropanoyl)-4-phenyl-2H-1-benzopyran-2-one is derived from natural sources and exhibits a range of biological activities, making it a potential candidate for various applications in the pharmaceutical and cosmetic industries.
Uses
Used in Pharmaceutical Industry:
5,7-Dihydroxy-8-(3-methyl-2-butenyl)-6-(2-methylpropanoyl)-4-phenyl-2H-1-benzopyran-2-one is used as a bioactive compound for its potential therapeutic effects. The compound's antioxidant and antimalarial properties make it a promising candidate for the development of new drugs to treat these conditions. Its ability to inhibit HIV-1 replication by targeting the NF-kappaB pathway also suggests its potential use in the development of antiretroviral medications.
Used in Cosmetic Industry:
In the cosmetic industry, 5,7-Dihydroxy-8-(3-methyl-2-butenyl)-6-(2-methylpropanoyl)-4-phenyl-2H-1-benzopyran-2-one is used as an active ingredient for its antioxidant properties. It can be incorporated into skincare products to protect the skin from oxidative stress and environmental damage, promoting a healthier and more youthful appearance.
Used in Drug Delivery Systems:
Similar to gallotannin, 5,7-Dihydroxy-8-(3-methyl-2-butenyl)-6-(2-methylpropanoyl)-4-phenyl-2H-1-benzopyran-2-one can also be used in the development of novel drug delivery systems. These systems can enhance the compound's bioavailability, delivery, and therapeutic outcomes, making it more effective in treating various conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 16981-20-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,9,8 and 1 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 16981-20:
(7*1)+(6*6)+(5*9)+(4*8)+(3*1)+(2*2)+(1*0)=127
127 % 10 = 7
So 16981-20-7 is a valid CAS Registry Number.
InChI:InChI=1/C24H24O5/c1-13(2)10-11-16-22(27)20(21(26)14(3)4)23(28)19-17(12-18(25)29-24(16)19)15-8-6-5-7-9-15/h5-10,12,14,27-28H,11H2,1-4H3
16981-20-7Relevant articles and documents
Synthesis of Mammea Coumarins. Part 1. The Coumarins of the Mammea A, B, and C Series
Crombie, Leslie,Jones, Raymond C. F.,Palmer, Christopher J.
, p. 317 - 332 (2007/10/02)
The naturally-occuring Mammea coumarins of the 4-phenyl-(mammea A), propyl-(mammea B), and 4-pentyl-(mammea C) series have been prepared by Pechmann condensation of an acylphloroglucinol (3-methylbutyryl-, 2-methylbutyryl-, butyryl-, or 2-methylpropionyl-) with the appropriate β-ketoester to give a mixture of 6- and 8-acyl-5,7-dihydroxycoumarins that could be separated.C-Alkylation with 3-methylbut-2-enyl bromide, or 3,7-dimethylocta-2,6-dienyl chloride, in aqueous potassium hydroxide completed the synthesis of the Mammea coumarins having unmodified prenyl or geranyl substituents; oxidative modification of the prenyl group led to the mammea cyclo E and cyclo F coumarins.Some mammea cyclo D (chromeno) coumarins were synthesized by reaction of acylcoumarins with 1,1-dimethoxy-3-methylbutan-3-ol.
