83967-05-9 Usage
Chemical class
Pyrimidine derivative
Cyclopentyl group
A five-membered ring with an alkyl substituent attached to the pyrimidine ring
Methylamino group
An amino group with a methyl group attached to the nitrogen atom
Hydroxy group
A hydroxyl (-OH) group attached to the cyclopentyl ring
Hydroxymethyl group
A -CH2OH group attached to the cyclopentyl ring
Potential applications
Pharmaceutical industry
Biological activity
Contains functional groups commonly found in biologically active compounds
Research interest
Medicinal chemistry and drug development
Unique structure
Combination of pyrimidine ring, cyclopentyl group, and functional groups (hydroxy, hydroxymethyl, and methylamino)
Check Digit Verification of cas no
The CAS Registry Mumber 83967-05-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,9,6 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 83967-05:
(7*8)+(6*3)+(5*9)+(4*6)+(3*7)+(2*0)+(1*5)=169
169 % 10 = 9
So 83967-05-9 is a valid CAS Registry Number.
83967-05-9Relevant academic research and scientific papers
Carbocyclic analogues of 5-substituted uracil nucleosides: Synthesis and antiviral activity
Shealy,O'Dell,Shannon,Arnett
, p. 156 - 161 (2007/10/02)
Carbocyclic analogues of 3'-deoxyuridines and uridines with substituents at position 5 of the uracil moiety were prepared by direct halogenation (5-bromo and 5-iodo groups) and by displacement of the 5-bromo group by amino and substituted-amino groups. The analogue of 5-(hydroxymethyl)uridine was prepared via reaction of the isopropylidene derivative of the uridine analogue with paraformaldehyde. The carbocyclic analogues of thymidine and of 5-bromo-, 5-iodo-, and 5-(methylamino)-2'-deoxyuridine were highly active in vitro against herpes simplex virus, types 1 and 2. The corresponding analogues of 5-substituted 3'-deoxyuridines and of 5-substituted uridines were not active in this assay.
