72429-30-2

Basic information

• Product Name: Cytidine, N-benzoyl-2',5'-bis-O-[(1,1-dimethylethyl)dimethylsilyl]-
• CAS NO: 72429-30-2
• Molecular Formula: C28H45N3O6Si2
• Molecular Weight: 575.853
• Mol File: 72429-30-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Cytidine, N-benzoyl-2',5'-bis-O-[(1,1-dimethylethyl)dimethylsilyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Cytidine, N-benzoyl-2',5'-bis-O-[(1,1-dimethylethyl)dimethylsilyl]-(72429-30-2)
• EPA Substance Registry System: Cytidine, N-benzoyl-2',5'-bis-O-[(1,1-dimethylethyl)dimethylsilyl]-(72429-30-2)

Safety Data

• Hazardous Substances Data: 72429-30-2(Hazardous Substances Data)

Upstream product

• 18162-48-6 tert-butyldimethylsilyl chloride 
• 3676-72-0 N²-benzoylguanosine 
• 13089-48-0 N₄-benzoylcytidine 

Downstream Products

• 142573-75-9 N⁴-benzoyl-1-[2',5'-bis-O-(tert-butyldimethylsilyl)-β-D-erythro-pentofuran-3'-ulosyl]cytosine 
• 72687-01-5 N-benzoyl-2'-O-(tert-butyldimethylsilyl)cytidine 
• 292042-79-6 N-{1-[3-(tert-butyl-dimethyl-silanyloxy)-5-(tert-butyl-dimethyl-silanyloxymethyl)-4-methylsulfanylmethoxy-tetrahydro-furan-2-yl]-2-oxo-1,2-dihydro-pyrimidin-4-yl}-benzamide 
• 674784-56-6 C₂₂H₃₀⁽²⁾HN₃O₆Si 
• 501014-33-1 N⁴-benzoyl-2'-O-(tert-butyldimethylsilyl)-3'-ketocytidine 

Relevant articles and documents

Chemical Synthesis of the Antiviral Nucleotide Analogue ddhCTP

3′-Deoxy-3′,4′-didehydro-cytidine triphosphate (ddhCTP) is a novel antiviral molecule produced by the enzyme viperin as part of the innate immune response. ddhCTP has been shown to act as an obligate chain terminator of flavivirus and SARS-CoV-2 RNA-depen

New catalists and procedures for the dimethoxytritylation and selective silylation of ribonucleosides

Procedures have been developed for the selective formation of (a) 2',5'-silylated ribonucleosides and (b) 3',5'-silylated ribonucleosides.These procedures also permit the selective silylation at either the 2'- or 3'-position of dimethoxytritylated ribonuc

NITRATE ION AS CATALYST FOR SELECTIVE SILYLATIONS OF NUCLEOSIDES

Nitrate ion has been found to have a remarkable effect on the selectivity of silylation of ribonucleosides using the t-butyldimethylsilyl group.