302790-83-6 Usage
Molecular structure
2,5-anhydro-3-deoxy-D-mannitol backbone with a 5-fluoro-3,4-dihydro-2,4-dioxo-1(2H)-pyrimidinyl moiety attached.
Derivative
It is a derivative of D-mannitol, a naturally occurring sugar alcohol.
Fluorinated pyrimidinyl group
The presence of this group imparts antiviral properties to the compound.
Antiviral activity
The compound has been studied for its potential to inhibit viral replication, making it a potential antiviral agent.
Pharmaceutical industry application
It is used in the pharmaceutical industry for its potential therapeutic applications.
Complex structure
The compound has a complex structure, which contributes to its unique properties and potential uses.
Further research needed
More research and development are required to fully understand its pharmacological properties and potential use in medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 302790-83-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,2,7,9 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 302790-83:
(8*3)+(7*0)+(6*2)+(5*7)+(4*9)+(3*0)+(2*8)+(1*3)=126
126 % 10 = 6
So 302790-83-6 is a valid CAS Registry Number.
302790-83-6Relevant articles and documents
Synthesis of 3-deoxy-3-nucleobase-2,5-anhydro-D-mannitol: A novel class of hydroxymethyl-branched isonucleosides
Lei,Min,Zhang
, p. 2899 - 2906 (2000)
A concise synthesis of 3-deoxy-3-nucleobase-2,5-anhydro-D-mannitol 6(a- d) has been achieved, using the deamination of 2-amino-2-deoxy-D-glucose to construct in one step the sugar skeleton with the desired sense of chirality at each asymmetric center. The selective dibenzoylation of 2,5-anhydro-D- mannitol 9 was investigated, and the key epoxide intermediate 13 was obtained in good yield via an intramolecular Mitsunobu reaction. The process of opening of epoxide 13 by nucleobases appeared to be regioselective. (C) 2000 Elsevier Science Ltd.
