2′,3′,5′-Tri-O-benzoyluridine is a modified nucleoside derivative of uridine, characterized by the presence of three benzoyl groups attached to the hydroxyl positions at the 2′, 3′, and 5′ positions of the ribose sugar. This modification enhances the lipophilicity and stability of the molecule, making it useful in various biochemical applications, including as a building block in oligonucleotide synthesis. The compound is typically a white to off-white solid and is soluble in organic solvents such as dichloromethane and acetone, but less soluble in water due to its hydrophobic nature. Its structure allows for potential interactions in biological systems, and it can be utilized in research related to nucleic acid chemistry and drug development. The presence of the benzoyl groups also provides sites for further chemical modifications, making it a versatile compound in synthetic organic chemistry. As with many nucleoside derivatives, it is important to handle this substance with care, following appropriate safety protocols.

2′,3′,5′-Tri-O-benzoyluridine

1748-04-5: 1-(2,3,5-tri-O-benzoylpentofuranosyl)pyrimidine-2,4(1H,3H)-dione, 2′,3′,5′-Tri-O-benzoyluridine, 2′,3′,5′-Tribenzoyluridine, NSC 97840, Uridine 2',3',5'-tribenzoate, Uridine, 2′,3′,5′-tribenzoate

2'',3'',5''-Tri-O-benzoyluridine

2',3',5'-Tri-O-benzoyluridine is a protected form of the nucleoside uridine. Uridine is a pyrimidine nucleoside consisting of uracil as the nitrogenous base and a ribose sugar linked via a β-N-glycosidic bond at the 1′ position. The hydroxyl groups on the ribose (at positions 2′, 3′, and 5′) are protected with benzoyl groups (-O-CO-C₆H₅).

CAS 1748-04-5: 2′,3′,5′-Tri-O-benzoyluridine

2'',3'',5''-Tri-O-benzoyluridine

Ref: 7W-GN1589

2',3',5'-Tri-O-benzoyluridine

Ref: 3D-NT08060