14985-34-3

Basic information

• Product Name: N(3)-benzyluridine
• Synonyms: N(3)-benzyluridine
• CAS NO: 14985-34-3
• Molecular Formula: C₁₆H₁₈N₂O₆
• Molecular Weight: 334.32392
• Mol File: 14985-34-3.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 589.1°Cat760mmHg
• Flash Point: 310.1°C
• Appearance: /
• Density: 1.525g/cm³
• Vapor Pressure: 1E-14mmHg at 25°C
• Refractive Index: 1.672
• PKA: 13.26±0.70(Predicted)
• CAS DataBase Reference: N(3)-benzyluridine(CAS DataBase Reference)
• NIST Chemistry Reference: N(3)-benzyluridine(14985-34-3)
• EPA Substance Registry System: N(3)-benzyluridine(14985-34-3)

Safety Data

• Hazardous Substances Data: 14985-34-3(Hazardous Substances Data)

Usage

InChI:InChI=1/C16H18N2O6/c19-9-11-13(21)14(22)15(24-11)17-7-6-12(20)18(16(17)23)8-10-4-2-1-3-5-10/h1-7,11,13-15,19,21-22H,8-9H2/t11-,13-,14-,15-/m1/s1

Upstream product

• 100-39-0 benzyl bromide 
• 58-96-8 uridine 
• 820212-17-7 N³,2',3'-tribenzyluridine 
• 820212-28-0 3-benzyl-1-[3,4-bis-benzyloxy-5-(tert-butyl-dimethyl-silanyloxymethyl)-tetrahydro-furan-2-yl]-1H-pyrimidine-2,4-dione 
• 100-44-7 benzyl chloride 
• 87418-77-7 5'-O-(tert-butyldimethylsilyl)uridine 
• 32464-90-7 N³-benzyl-2',3'-O-isopropylideneuridine 

Relevant articles and documents

Nucleosides. XVII. Benzylation-debenzylation studies on nucleosides

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Simultaneous removal of benzyl and benzyloxycarbonyl protective groups in 5′-O-(2-deoxy-α-D-glucopyranosyl)uridine by catalytic transfer hydrogenolysis

Synthesis of N3,2′,3′-O-tris-(benzyloxycarbonyl)uridine and its use in the synthesis of 5′-O-(2-deoxy-α-d-glucopyranosyl)uridine is described. Simultaneous removal of benzyl and benzyloxycarbonyl groups was accomplished by catalytic transfer hydrogenolysis in the presence of Pearlman′s catalyst without competing side reactions. Copyright Taylor & Francis Group, LLC.

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

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