83644-00-2 Usage
Uses
Used in Pharmaceutical Industry:
Rooperol is used as an anti-inflammatory agent for its ability to reduce inflammation, which can be beneficial in treating various inflammatory conditions.
Rooperol is used as an antioxidant for its capacity to neutralize harmful free radicals, potentially contributing to the prevention of oxidative stress-related diseases.
Used in Oncology:
Rooperol is used as an anti-cancer agent for its demonstrated effects on inhibiting the growth and metastasis of cancer cells, making it a candidate for further research in cancer treatment.
Used in Neurodegenerative Disease Treatment:
Rooperol is used as a neuroprotective agent due to its potential to protect neurons from damage, suggesting its use in the treatment of neurodegenerative diseases such as Alzheimer's and Parkinson's.
Check Digit Verification of cas no
The CAS Registry Mumber 83644-00-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,6,4 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 83644-00:
(7*8)+(6*3)+(5*6)+(4*4)+(3*4)+(2*0)+(1*0)=132
132 % 10 = 2
So 83644-00-2 is a valid CAS Registry Number.
83644-00-2Relevant academic research and scientific papers
A concise synthesis of rooperol and related 1,5-diarylpent-1-en-4-ynes
Kerwin, Sean M.,Cha, Jonathan
supporting information, p. 137 - 141 (2014/01/06)
Two powerful strategies: rapid construction of allylic alkynoates via cyclopropenium ion chemistry and mild, palladium-catalyzed decarboxylative coupling were employed in a concise, 5-steps synthesis of the natural product rooperol. The overall approach a
SYNTHESIS OF ROOPEROL
Potgieter, Maudene,Wenteler, George L.,Drewes, Siegfried E.
, p. 1101 - 1104 (2007/10/02)
Rooperol, a phenolic compound bearing the pentenyne moiety, has been synthesized from simple starting materials via a nine step synthesis.A crucial step in the synthesis involves protection of the phenolic groups as the tertbutyldimethylsilyl ether deriva
