55018-48-9

Basic information

• Product Name: 2,3,5-tri-O-benzoyl-1-deoxy-D-ribofuranose
• CAS NO: 55018-48-9
• Molecular Weight: 446.456
• Mol File: 55018-48-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2,3,5-tri-O-benzoyl-1-deoxy-D-ribofuranose(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3,5-tri-O-benzoyl-1-deoxy-D-ribofuranose(55018-48-9)
• EPA Substance Registry System: 2,3,5-tri-O-benzoyl-1-deoxy-D-ribofuranose(55018-48-9)

Safety Data

• Hazardous Substances Data: 55018-48-9(Hazardous Substances Data)

Upstream product

• 420-37-1 trimethoxonium tetrafluoroborate 
• 98-88-4 benzoyl chloride 
• 491-19-0 1,4-anhydro-D-ribitol 
• 14215-97-5 1-O-acetyl-2,3,5-tri-O-benzoyl-D-ribofuranose 
• 6974-32-9 1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose 
• 87-99-0 XYLITOL 
• 491-19-0 (2RS, 3RS, 4SR)-2-(hydroxymethyl)tetrahydrofuran-3,4-diol 
• 488-81-3 Adonitol 
• 491-19-0 1,4-anhydro-D,L-ribitol 

Downstream Products

• 14233-62-6 2,3,5-tri-O-benzyl-1-deoxy-D-ribofuranose 
• 491-19-0 1,4-anhydro-D-ribitol 
• 159299-28-2 1-deoxy-5-O-(4,4'-dimethoxytrityl)-D-ribofuranose 

Relevant articles and documents

S-ANTIGEN TRANSPORT INHIBITING OLIGONUCLEOTIDE POLYMERS AND METHODS

Various embodiments provide STOPS? polymers that are S-antigen transport inhibiting oligonucleotide polymers, processes for making them and methods of using them to treat diseases and conditions. In some embodiments the STOPS? modified oligonucleotides include an at least partially phosphorothioated sequence of alternating A and C units having modifications as described herein. The sequence independent antiviral activity against hepatitis B of embodiments of STOPS? modified oligonucleotides, as determined by HBsAg Secretion Assay, is an EC50 that is less than 100 nM.

Synthesis and characterization of authentic standards for the analysis of ribofuranose-containing carbohydrates by the reductive-cleavage method

Described herein is the synthesis of all positional isomers of partially methylated and acetylated or benzoylated 1,4-anhydro-D-ribitol.The benzoates are generated simultaneously from 1,4-anhydro-D-ribitol by sequential partial methylation and benzoylation or sequential partial benzoylation and methylation.The individual isomers are obtained in pure form by high-performance liquid chromatography.Debenzoylation and acetylation provided the corresponding acetates.Reported herein are the 1H NMR spectra of the benzoates and the electron-ionization mass spectra of the acetates and the tri-O-methyl derivative and also for the acetates and the tri-O-methyl derivative, their linear temperature programmed gas-liquid chromatography retention indices on three different capillary columns.Keywords: Reductive-cleavage; D-Ribitol, 1,4-anhydro, partially methylated and acylated

Transformations of β-Glycofuranosyl Isocyanides into Tetrahydrofurans

Readily available β-glycofuranosyl isocyanides 1, 2, 4, 5, 6, 18, 19, 20 are transformed into the corresponding protected tetrahydrofurans 21, 22, 23, 24, 25, 26 by means of tributyltin hydride and AIBN.The synthesis of 18 and 19 by dehydration of the for