62102-31-2 Usage
Type
Synthetic nucleoside analog
Function
Antiviral properties
Mechanism of Action
Interferes with the replication of viral genetic material
Effective against
Hepatitis C, respiratory syncytial virus (RSV), and other viral infections
Administration
Oral, injection, or inhaled
Combination Therapy
Often used with other antiviral medications to enhance effectiveness
Side Effects
Anemia, fatigue, nausea
Monitoring
Healthcare providers and patients should carefully monitor and manage potential complications during treatment
Check Digit Verification of cas no
The CAS Registry Mumber 62102-31-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,1,0 and 2 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 62102-31:
(7*6)+(6*2)+(5*1)+(4*0)+(3*2)+(2*3)+(1*1)=72
72 % 10 = 2
So 62102-31-2 is a valid CAS Registry Number.
62102-31-2Relevant articles and documents
Rapid synthesis of (±)-r-7-benzyloxymethyl-cyclopenta-cis-[4,5][1,3]-oxazolo[3,2-a] pyrimidinones versatile carbocyclic nucleoside precursors
Pérez, Nury,Gordillo, Barbara
, p. 671 - 676 (2007/10/03)
(±)-r-7-Benzyloxymethyl-cyclopenta-cis-[4,5][1,3]-oxazolo[3,2-a] pyrimidinones were synthesized in two steps from 1-hydroxymethyl-3-cyclopentene. These compounds are versatile intermediates for the synthesis of carbocyclic nucleosides. The synthesis has been accomplished by the iodofunctionalization of olefins as a method of coupling the pyrimidine bases and the carbocycle.
Regiospecific synthesis of cyclopentane analogs of (2'- and 3'-deoxy-threo-pentofuranosyl)-uracil and -2-thiouracil nucleosides
Hronowski,Szarek
, p. 2787 - 2797 (2007/10/02)
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