23722-97-6 Usage
Molecular Structure
Contains a purine base and a cyclopentanol group.
Purine Base
Derivative of adenine, a component of DNA and RNA.
Cyclopentanol Group
Five-membered ring with a hydroxymethyl substituent.
Potential Applications
May have applications in pharmaceuticals.
Biological Activity
Purine derivatives are known to have biological activity, including as anti-cancer and anti-viral agents.
Reactivity
Presence of the hydroxymethyl group suggests potential reactivity for further functionalization and modification.
Versatility
Shows promise as a versatile and potentially valuable chemical compound in the field of medicinal chemistry and drug development.
Check Digit Verification of cas no
The CAS Registry Mumber 23722-97-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,7,2 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 23722-97:
(7*2)+(6*3)+(5*7)+(4*2)+(3*2)+(2*9)+(1*7)=106
106 % 10 = 6
So 23722-97-6 is a valid CAS Registry Number.
23722-97-6Relevant articles and documents
(±)-3'-Deoxyaraaristeromycin via a surprising rearrangement
Frick,Patil,Gambino,Schneller
, p. 5541 - 5544 (2007/10/02)
Hydrolysis of (±)-3β-acetoxy-4α-benzamido-1α-cyclopentanemethyl acetate (5) with 6 N hydrochloric acid has been found to give an amine in which the configuration at C-3 has been inverted. This conclusion was reached following conversion of the amine into (±)-3'-deoxyaraaristeromycin (8) by following a standard adenine formation process of (i) reaction with 5-amino-4,6-dichloropyrimidine, (ii) ring closure with diethoxymethyl acetate, and (iii) ammonolysis. Use of basic hydrolysis conditions with 5 led to the expected (±)-3'-deoxyaristeromycin (7).
