58479-65-5

Basic information

• Product Name: 5'-O-(tert-butyldiphenylsilyl)cytidine
• Synonyms: 5'-O-(tert-butyldiphenylsilyl)cytidine
• CAS NO: 58479-65-5
• Molecular Weight: 481.624
• Mol File: 58479-65-5.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 5'-O-(tert-butyldiphenylsilyl)cytidine(CAS DataBase Reference)
• NIST Chemistry Reference: 5'-O-(tert-butyldiphenylsilyl)cytidine(58479-65-5)
• EPA Substance Registry System: 5'-O-(tert-butyldiphenylsilyl)cytidine(58479-65-5)

Safety Data

• Hazardous Substances Data: 58479-65-5(Hazardous Substances Data)

Upstream product

• 58479-61-1 tert-butylchlorodiphenylsilane 
• 65-46-3 CYTIDINE 

Downstream Products

• 1415645-50-9 7-O-(tert-butyldiphenylsilyl)morpholinocytidine 
• 160905-83-9 4-N-benzoyl-5'-O-(tert-butyldiphenylsilyl)-2',3'-bis-O-(9-phenylxanthen-9-yl)cytidine 
• 220765-73-1 C₄₄H₅₅N₄O₂₄P 
• 194665-67-3 allyl 2',3'-O,N⁴-triacetylcytidin-5'-yl methyl 4,7,8,9-tetra-O-acetyl-5-amino-5-N-benzyloxycarbonyl-3,5-dideoxy-β-D-glycero-D-galacto-2-nonulopyranosid-2''-yl phosphite 
• 194665-69-5 2',3'-O,N⁴-triacetylcytidin-5'-yl methyl 4,7,8,9-tetra-O-acetyl-5-amino-5-N-benzyloxycarbonyl-3,5-dideoxy-β-D-glycero-D-galacto-2-nonulopyranosid-2''-yl phosphate 
• 135546-48-4 cytidin-5'-yl 5-N-carbobenzyloxyamino-3,5-dideoxy-β-D-glycero-D-galacto-2-nonulopyranosid-2''-yl phosphate 
• 98300-80-2 2-O-(cytidin-5'-yloxyphosphoryl)-5-(2-hydroxy-acetamido)-3,5-dideoxy-β-D-glycero-D-galacto-2-nonulopyranosonic acid 
• 302346-93-6 3-propenyl (2',3'-O,N⁴-tribenzoyl cytidine-5')-yl (methyl (5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-2-thio-β-D-glycero-D-galacto-2-nonulopyranosid-2))-yl phosphorothioate 
• 302346-91-4 3-propenyl-(2',3'-O,N⁴-tribenzoyl cytidine-5')-yl-N,N'-diisopropylphosphoramidite 
• 54898-05-4 N,2',3'-O-tribenzoylcytidine 
• 302346-90-3 2',3'-O,N⁴-tribenzoyl-5'-O-tert-butyldiphenylsilyl cytidine 
• 194665-58-2 2',3'-O,N⁴-triacetyl-5'-tert-butyldiphenylsilyl cytidine 
• 134821-65-1 4-N-benzoyl-1-(5-O-tert-butyldiphenylsilyl-β-D-ribofuranosyl)cytosine 

Relevant articles and documents

Synthesis and in vitro growth inhibitory activity of novel silyl- and trityl-modified nucleosides

Seventeen silyl- and trityl-modified (5′-O- and 3′,5′-di-O-) nucleosides were synthesized with the aim of investigating the in vitro antiproliferative activities of these nucleoside derivatives. A subset of the compounds was evaluated at a fixed concentra

Selective inhibitors of bacterial phosphopantothenoylcysteine synthetase

(Figure Presented) Bacterial phosphopantothenolycysteine synthetase (PPCS) catalyzes the formation of phosphopantothenoylcysteine (PPC) from (R)-phosphopantothenate, L-cysteine, and cytidine-5′-triphosphate (CTP) and has been shown to be essential for gro

Synthesis of CMP-sialic acid conjugates: Substrates for the enzymatic synthesis of natural and designed sialyl oligosaccharides

The syntheses of several congeners of CMP-NeuAc are described. These compounds are substrates for enzymatic glycosylation.