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Uridine 3-(phenylmethyl)-2',3',5'-triacetate is a chemical compound derived from the nucleoside uridine, which is a component of RNA. This specific compound is characterized by the presence of a phenylmethyl group attached to the uridine molecule and three acetate groups esterified to the 2', 3', and 5' positions of the ribose sugar moiety. The phenylmethyl group provides a hydrophobic character to the molecule, while the acetate groups increase its stability and solubility in organic solvents. Uridine, 3-(phenylmethyl)-, 2',3',5'-triacetate is often used in biochemical research and as a building block in the synthesis of more complex nucleic acid derivatives, due to its unique structure and reactivity.

93960-47-5

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93960-47-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93960-47-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,9,6 and 0 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 93960-47:
(7*9)+(6*3)+(5*9)+(4*6)+(3*0)+(2*4)+(1*7)=165
165 % 10 = 5
So 93960-47-5 is a valid CAS Registry Number.

93960-47-5Relevant academic research and scientific papers

Synthesis and hypnotic activities of 4-thio analogues of N3-substituted uridines

Kozai,Maruyama,Kimura,Yamamoto

, p. 1185 - 1188 (2007/10/03)

Reaction of tri-O-acetyluridine (1) with benzyl bromide or 2-chloroacetophenone in the presence of K2CO3 gave the N3-substituted analogues 2a,c. Condensation of 1 with (±)-1-phenylethanol or 3,5-dimethylbenzyl alcohol usin

N-Substituted Oxopyrimidines and Nucleosides: Structure-Activity Relationship for Hypnotic Activity as Central Nervous System Depressant

Yamamoto, Ikuo,Kimura, Toshiyuki,Tateoka, Yuji,Watanabe, Kazuhito,Ho, Ing Kang

, p. 2227 - 2231 (2007/10/02)

N3-Benzyluridine (3-(phenylmethyl)-1-β-D-ribofuranosyluracil) (1f) and its related compounds were synthesized and evaluated for hypnotic activity as central depressants.The primary structural modification has been carried out at the N3/su

AN EFFECTIVE METHOD FOR THE PREPARATION OF O6-SUBSTITUTED GUANOSINE AND N3-SUBSTITUTED URIDINE DERIVATIVES VIA THE CORRESPONDING STANNYLATED INTERMEDIATES

Tanimura, Hiroshi,Sekine, Mitsuo,Hata, Tsujiaki

, p. 4047 - 4050 (2007/10/02)

O6-substituted guanosine and N3-substituted uridine derivatives were obtained in high yields by stannylation of the corresponding unsubstituted nucleosides with bis(tributyltin)-oxide followed by treatment with various electrophiles.

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