41545-90-8

Basic information

• Product Name: 1-(O³,O⁵-dibenzoyl-α-L-erythro-2-deoxy-pentofuranosyl)-1H-pyrimidine-2,4-dione
• CAS NO: 41545-90-8
• Molecular Weight: 436.421
• Mol File: 41545-90-8.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: 1-(O³,O⁵-dibenzoyl-α-L-erythro-2-deoxy-pentofuranosyl)-1H-pyrimidine-2,4-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(O³,O⁵-dibenzoyl-α-L-erythro-2-deoxy-pentofuranosyl)-1H-pyrimidine-2,4-dione(41545-90-8)
• EPA Substance Registry System: 1-(O³,O⁵-dibenzoyl-α-L-erythro-2-deoxy-pentofuranosyl)-1H-pyrimidine-2,4-dione(41545-90-8)

Safety Data

• Hazardous Substances Data: 41545-90-8(Hazardous Substances Data)

Upstream product

• 4104-89-6 triphenylpropargyl stannane 
• 62232-29-5 3',5'-di-O-benzoyl-2'-bromo-2'-deoxyuridine 
• 24850-33-7 allyltributylstanane 
• 31616-01-0 3’,5’-O-benzoyl-2,2’-anhydrouridine 
• 10457-14-4 O,O'-bis-(trimethylsilyl)uracil 
• 613-90-1 benzoyl cyanide 
• 22224-41-5 1,3,5-tri-O-benzoyl-α-D-ribofuranoside 
• 145828-13-3 α-D-1,3,5-tri-O-benzoyl-2-O-[3-(trifluoromethyl)benzoyl]ribofuranose 
• 98-88-4 benzoyl chloride 
• 3992-42-5 2'-deoxycytidine monohydrochloride 
• 31501-22-1 N⁴-benzoyl-1-(3',5'-di-O-benzoyl-2'-deoxy-β-D-ribofuranosyl)-cytosine 
• 89480-34-2 2,3'-Anhydro-1-(2-desoxy-5-O-benzoyl-β-D-xylofuranosyl)-uracil 
• 182004-58-6 3',5'-di-O-benzoyl-2'-O-[3-(trifluoromethyl)benzoyl]uridine 
• 175024-33-6 C₂₃H₂₉N₂O₇P 

Downstream Products

• 139954-93-1 C₂₆H₂₁F₃N₂O₇ 
• 1161403-57-1 3',5'-di-O-benzoyl-2'-deoxy-5-methylselenyluridine 
• 2691-71-6 C₂₃H₁₉FN₂O₇ 
• 135080-78-3 1-((2R,4S,5R)-4-Hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-3-(4-methoxy-benzyl)-1H-pyrimidine-2,4-dione 
• 123606-62-2 5'-O-Benzoyl-2'-desoxy-β-D-ribofuranosyluracil 
• 135080-77-2 C₃₁H₂₈N₂O₈ 

Relevant articles and documents

A general method for N-glycosylation of nucleobases promoted by (p-Tol)2SO/Tf2O with thioglycoside as donor

Based on a preactivation strategy using the (p-Tol)2SO/Tf2O system, a series of nucleosides were synthesized by coupling various thioglycosides with pyrimidines and purines under mild conditions. High yields and excellent β-stereoselectivities were obtained with either armed or disarmed N-glycosylation donors by tuning the amount of (p-Tol)2SO additive.

Continuous flow photocatalysis enhanced using an aluminum mirror: Rapid and selective synthesis of 2′-deoxy and 2′,3′-dideoxynucleosides

A unique photochemical flow reactor featuring quartz tubing, an aluminum mirror and temperature control has been developed for the photo-induced electron-transfer deoxygenation reaction to produce 2′-deoxy and 2′,3′-dideoxynucleosides. The continuous flow format significantly increased the efficiency and selectivity of the reaction.

5-(E)-Bromovinyl uracil analogues and related pyrimidine nucleosides as anti-viral agents and methods of use

The present invention relates to pyrimidine nucleoside compounds and their use to treat viral infections of Varicella Zoster virus and Epstein Barr Virus, as well as cancers which are complications of Epstein Barr virus.