72323-54-7 Usage
Structure
Heterocyclic compound with a bicyclic structure
Substituents
Fluoro group (6-fluoro)
Pentyl group (8-pentyl)
Derivative of
Diazabicyclooctane
Activity
Potent inhibitor of the enzyme fatty acid amide hydrolase
Biological Target
Fatty acid amide hydrolase, part of the endocannabinoid system
Potential Applications
Development of new drugs for neurological disorders
Pain management
Research Need
Additional research required to fully understand properties and potential uses.
Check Digit Verification of cas no
The CAS Registry Mumber 72323-54-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,3,2 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 72323-54:
(7*7)+(6*2)+(5*3)+(4*2)+(3*3)+(2*5)+(1*4)=107
107 % 10 = 7
So 72323-54-7 is a valid CAS Registry Number.
72323-54-7Relevant academic research and scientific papers
Anion-Mediated Fragmentation Reactions. Mechanistic and Synthetic Aspects of the Fragmentation and Rearrangement Reactions of Pyrimidinedione-Alkyne Photoadducts
Kaminski, Victor V.,Comber, Robert N.,Wexler, Allan J.,Swenton, John S.
, p. 2337 - 2346 (2007/10/02)
The acetone-sensitized photocycloadditon reactions of uracil, thymine, 5-fluorouracil, and 5-(trimethylsilyl)uracil with alkynes afford 2,4-diazabicyclooct-7-ene-3,5-diones.It is noteworthy that 5-(trimethylsilyl)uracil gives very high yields in th
