188754-55-4 Usage
General Description
Uridine, 5-methyl-, 2'-acetate 3',5'-dibenzoate is a compound that is derived from uridine, a nucleoside that plays a crucial role in various biological processes. The 2'-acetate 3',5'-dibenzoate modification of uridine adds two benzene rings to the molecule, which can affect its chemical and biological properties. Uridine, 5-methyl-, 2'-acetate 3',5'-dibenzoate may have potential applications in research related to nucleoside chemistry and biochemistry. Its unique structure and properties make it a valuable tool for studying the functions and interactions of uridine and related compounds in biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 188754-55-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,7,5 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 188754-55:
(8*1)+(7*8)+(6*8)+(5*7)+(4*5)+(3*4)+(2*5)+(1*5)=194
194 % 10 = 4
So 188754-55-4 is a valid CAS Registry Number.
188754-55-4Relevant articles and documents
Stereocontrolled Syntheses of Deoxyribonucleosides via Photoinduced Electron-Transfer Deoxygenation of Benzoyl-Protected Ribo- and Arabinonucleosides
Wang, Zhiwei,Prudhomme, Daniel R.,Buck, Jason R.,Park, Minnie,Rizzo, Carmelo J.
, p. 5969 - 5985 (2007/10/03)
The stereocontrolled, de novo syntheses of β-2′-deoxy-, α-2′-deoxy-, β-3′-deoxy-, and β-2′,3′-dideoxyribonucleosides are described. Strategically protected ribose, arabinose, and xylose glycosylation precursors were synthesized bearing C2-esters capable of directing Vorbrueggen glycosylation. The key step is the regioselective deoxygenation of the desired hydroxyl group as either the benzoyl- or 3-(trifluoromethyl)benzoyl derivative. This deoxygenation is accomplished via a photoinduced electron-transfer (PET) mechanism using carbazole derivatives as the photosensitizer. The syntheses of the desired deoxynucleoside generally proceed in three steps from a common, readily available precursor.
