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Uridine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl], 2'-(4-oxopentanoate) is a complex organic compound with the molecular formula C31H33N2O9. It is a derivative of uridine, a nucleoside composed of uracil and ribose, which plays a crucial role in RNA synthesis. In this specific compound, the uridine molecule is modified with a 5'-O-[bis(4-methoxyphenyl)phenylmethyl] group and a 2'-(4-oxopentanoate) group. The 5'-O-[bis(4-methoxyphenyl)phenylmethyl] group is a bulky, electron-rich aryl moiety that can influence the compound's interactions with enzymes and other biomolecules. The 2'-(4-oxopentanoate) group is a five-carbon ketone chain attached to the ribose sugar, which can further modulate the compound's properties. This chemical structure may be of interest in medicinal chemistry and drug development, as it could potentially alter the activity or specificity of uridine in biological systems.

96026-67-4

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96026-67-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96026-67-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,0,2 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 96026-67:
(7*9)+(6*6)+(5*0)+(4*2)+(3*6)+(2*6)+(1*7)=144
144 % 10 = 4
So 96026-67-4 is a valid CAS Registry Number.

96026-67-4Relevant academic research and scientific papers

Solid-phase synthesis and on-column deprotection of RNA from 2′- (and 3′-) O-Levulinated (Lv) ribonucleoside monomers

Lackey, Jeremy G.,Sabatino, David,Damha, Masad J.

, p. 789 - 792 (2008/01/27)

(Chemical Equation Presented) The solid-phase synthesis of oligoribonucleotides derived from ribonucleosides esterified at the 2′ (or 3′-) position with the levulinyl (Lv) group is described. The oligomers can be released from the solid support as 2′-O-Lv

Hydrolytic stability of a phosphate-branched oligonucleotide incorporating a ribonucleoside 3′-phosphotriester unit

Loennberg, Tuomas

, p. 315 - 323 (2007/10/03)

A phosphate-branched oligonucleotide has been prepared by using an appropriately protected trinucleoside phosphotriester building block in conventional solid-phase synthesis. Hydrolysis of the branched oligonucleotide has been followed over a wide pH range. Comparison of the present results with those previously obtained for simpler analogues indicates that a trinucleoside 3′,3′,5′-monophosphate, when embedded in an oligonucleotide structure, is stabilized toward hydroxide-ion catalyzed cleavage by more than one order of magnitude, lending some support to the feasibility of existence of phosphate-branched RNA X in biological systems. Copyright Taylor & Francis Group, LLC.

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