86654-26-4 Usage
Uses
Used in Pharmaceutical Industry:
7-Hydroxy-3-prenylcoumarin is used as a potential therapeutic agent for its various biological activities. Its antioxidant properties make it a candidate for the treatment of oxidative stress-related diseases, while its anti-inflammatory effects could be beneficial in managing inflammatory conditions.
7-Hydroxy-3-prenylcoumarin is also used as an anti-cancer agent due to its ability to target and inhibit the growth of cancer cells. Its potential to act against various types of cancer makes it a valuable compound for further research and development in oncology.
Used in Cosmetic Industry:
7-Hydroxy-3-prenylcoumarin can be used as an active ingredient in cosmetic products for its antioxidant and anti-inflammatory properties. It may help protect the skin from oxidative damage and reduce inflammation, contributing to healthier and more youthful-looking skin.
Used in Nutraceutical Industry:
As a compound with potential health benefits, 7-Hydroxy-3-prenylcoumarin can be incorporated into nutraceutical products, such as dietary supplements and functional foods. Its antioxidant and anti-inflammatory properties may provide additional health benefits when consumed as part of a balanced diet.
Check Digit Verification of cas no
The CAS Registry Mumber 86654-26-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,6,5 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 86654-26:
(7*8)+(6*6)+(5*6)+(4*5)+(3*4)+(2*2)+(1*6)=164
164 % 10 = 4
So 86654-26-4 is a valid CAS Registry Number.
86654-26-4Relevant academic research and scientific papers
Short synthesis of 3-prenylcoumarins by an unusual prenylation
Ramachandra, Marellapudi S.,Subbaraju, Gottumukkala V.
, p. 3723 - 3727 (2007/10/03)
Prenylation of coumarins that have hydroxyl or alkoxyl or halo substitution (1a-1i) using 2-methyl-3-butene-2-ol in the presence of boron trifluoride formed 3-prenylcoumarins (2a-2d). Copyright Taylor & Francis Group, LLC.
Synthesis of 3-(3,3-Dimethyl)xanthyletin
Swaroop, Divya,Sharma, R. B.,Kapil, R. S.
, p. 105 - 108 (2007/10/02)
A convenient method for the construction of 3,3-dimethylallyl unit at C-3 of coumarin nucleus has been developed and utilized in the synthesis of the title compound (14).The synthetic strategy involves condensation of 3-formyl-7-benzyloxycoumarin with ace
Synthesis of Balsamiferone and dl-3-(3,3-Dimethylallyl)marmesin
Swaroop, (KM) Divya,Sharma, R. B.,Kapil, R. S.
, p. 408 (2007/10/02)
The structures of naturally occurring coumarins balsamiferone and 3-(3,3-dimethylallyl)marmesin as 3,6-bis(3-methyl-2-butenyl)-7-hydroxycoumarin and 3-(3-methyl-2-butenyl)-6,7-dihydro-7-(1-hydroxy-1-methylethyl)-2H-furobenzopyran-2-one, respectively have been confirmed by syntheses.
