157953-22-5 Usage
Uses
Used in Pharmaceutical Applications:
Ethanone, 1-[3-(3-hydroxy-3-methyl-1-butynyl)-4-(phenylmethoxy)phenyl]is used as a potential therapeutic agent for its antioxidant, anti-inflammatory, and anti-cancer properties. It is being investigated for its potential to treat various diseases, including cancer, neurodegenerative disorders, and cardiovascular diseases.
Used in Research and Development:
In the field of scientific research, Ethanone, 1-[3-(3-hydroxy-3-methyl-1-butynyl)-4-(phenylmethoxy)phenyl]is used as a subject of study to explore its biological activities and potential medical applications. Ethanone,
1-[3-(3-hydroxy-3-methyl-1-butynyl)-4-(phenylmethoxy)phenyl]is of interest to researchers due to its complex molecular structure and the possibility of harnessing its properties for therapeutic purposes.
Used in Drug Discovery:
Ethanone, 1-[3-(3-hydroxy-3-methyl-1-butynyl)-4-(phenylmethoxy)phenyl]is utilized in drug discovery processes as a potential lead compound. Its unique structure and the observed biological activities make it a candidate for further development into a drug that could be used in the treatment of various diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 157953-22-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,7,9,5 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 157953-22:
(8*1)+(7*5)+(6*7)+(5*9)+(4*5)+(3*3)+(2*2)+(1*2)=165
165 % 10 = 5
So 157953-22-5 is a valid CAS Registry Number.
157953-22-5Relevant academic research and scientific papers
REGIOSELECTIVE PRENYLATION OF PHENOLS BY PALLADIUM CATALYST: SYNTHESES OF PRENYLPHENOLS AND CHROMANS
Tsukayama, Masao,Kikuchi, Makoto,Kawamura, Yasuhiko
, p. 1487 - 1490 (2007/10/02)
The palladium-catalyzed coupling reaction of iodophenols (1) with 2-methyl-3-butyn-2-ol gave alkynylphenols (2).Catalytic hydrogenation of 2 over Raney nickel and the subsequent dehydration of the resultant alkylphenols (3) gave regioselectively the desired prenylphenols (4).Dehydration of alkylphenols (3f-h) gave chromans (7).
