175013-46-4 Usage
Description
(2R,3R,3aS)-2-[(tert-butyldiphenylsilyl)oxy]methyl3-hydroxy-2,3,3a,9a-tetrahydro-6H-furo[2’,3’:4,5]oxazole[3,2a]-pyrimidin-6-one is a complex organic molecule with a chiral configuration of 2R,3R,3aS. It features a furoxan ring fused to a pyrimidine ring, along with a hydroxyl group and a tert-butyldiphenylsilyloxy functional group attached to its carbon atoms. This unique structure endows the compound with potential biological activities, making it a promising candidate for pharmaceutical research and drug development.
Uses
Used in Pharmaceutical Research:
(2R,3R,3aS)-2-[(tert-butyldiphenylsilyl)oxy]methyl3-hydroxy-2,3,3a,9a-tetrahydro-6H-furo[2’,3’:4,5]oxazole[3,2a]-pyrimidin-6-one is utilized as a research compound for exploring its potential biological activities and therapeutic effects. Its unique structure allows scientists to investigate its interactions with biological targets and evaluate its efficacy in treating various diseases.
Used in Drug Development:
In the pharmaceutical industry, (2R,3R,3aS)-2-[(tert-butyldiphenylsilyl)oxy]methyl3-hydroxy-2,3,3a,9a-tetrahydro-6H-furo[2’,3’:4,5]oxazole[3,2a]-pyrimidin-6-one serves as a lead compound for the development of new drugs. Its chiral configuration and functional groups can be further modified to optimize its pharmacological properties, such as potency, selectivity, and bioavailability, ultimately leading to the creation of novel therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 175013-46-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,0,1 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 175013-46:
(8*1)+(7*7)+(6*5)+(5*0)+(4*1)+(3*3)+(2*4)+(1*6)=114
114 % 10 = 4
So 175013-46-4 is a valid CAS Registry Number.
175013-46-4Relevant articles and documents
Synthesis of a protected keto-lysidine analogue via improved preparation of arabino-isocytosine nucleosides
Sweeney, Joseph B.,Bethel, Paul A.,Gill, Duncan M.,Ochocińska, Agata M.,Walsh, Anthony E.J.,Walton, Scarlett M.
supporting information, p. 2004 - 2007 (2019/04/10)
Anhydrouridines react with aliphatic amines to give N-alkyl isocytosines, but reported procedures often demand very long reaction times and can be low yielding, with narrow scope. A modified procedure for such reactions has been developed, using microwave
