174497-93-9

Upstream product

• 4756-05-2 thioacetone 
• 69304-38-7 3',5'-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)uridine 
• 75-18-3 dimethylsulfide 

Downstream Products

• 929896-78-6 C₂₉H₄₅N₃O₁₀Si₂ 
• 1020100-86-0 3',5'-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-2'-O-[[[4-[N-(dichloroacetyl)-N-methylamino]benzyl]oxy]methyl]uridine 
• 1344122-70-8 2'-O-(2,2-difluoro)ethoxymethyl-5'-O-(4,4'-dimethoxytrityl)uridine 
• 1344122-71-9 2'-O-(2,2,2-trifluoro)ethoxymethyl-5'-O-(4,4'-dimethoxytrityl)uridine 
• 1344122-72-0 C₄₂H₅₃N₄O₁₀P 
• 1344122-73-1 2'-O-(2-chloro)ethoxymethyl-5'-O-(4,4'-dimethoxytrityl)uridine 3'-(2-cyanoethyldiisopropylphosphoramidite) 
• 1344122-74-2 2'-O-(2,2-dichloro)ethoxymethyl-5'-O-(4,4'-dimethoxytrityl)uridine 3'-(2-cyanoethyldiisopropylphosphoramidite) 
• 1344122-75-3 2'-O-(2,2,2-trichloro)ethoxymethyl-5'-O-(4,4'-dimethoxytrityl)uridine 3'-(2-cyanoethyldiisopropylphosphoramidite) 
• 1344122-76-4 2'-O-(2,2-difluoro)ethoxymethyl-5'-O-(4,4'-dimethoxytrityl)uridine 3'-(2-cyanoethyldiisopropylphosphoramidite) 
• 1344122-77-5 2'-O-(2,2,2-trifluoro)ethoxymethyl-5'-O-(4,4'-dimethoxytrityl)uridine 3'-(2-cyanoethyldiisopropylphosphoramidite) 
• 81246-79-9 5'-dimethoxytrityluridine 
• 1276668-47-3 2'-O-(2-Trifluoromethyl-3,3,3-trifluoropropanoxymethyl)-5'-O-(4,4'-dimethoxytrityl)uridine 
• 1276668-49-5 2'-O-(2-Trifluoromethyl-3,3,3-trifluoropropanoxymethyl)-5'-O-(4,4'-dimethoxytrityl)uridine 3'-O-(2-cyanoethyl N,N-diisopropylphosphoramidite) 
• 1276668-59-7 5'-O-(4,4'-dimethoxytrityl)-2'-O-,3'-O-bis(benzyloxycarbonyl)uridine 

Relevant academic research and scientific papers

2'-O-methylthiomethyl modifications in hammerhead ribozymes

The synthesis of all four phosphoramidites of 2'-O-methylthiomethyl ribonucleosides and their incorporation into hammerhead ribozymes and influence on nuclease stability and catalytic activity is described.

Synthesis and Properties of 2'-O-Methoxymethyl Oligonucleotides

2'-O-Methoxymethyluridine was synthesized under mild conditions using N-iodosuccinimide (NIS) activation of a 2'-methoxythiomethyl function in presence of methanol.Oligoribonucleotides containing such modified uridine residues had slightly decreased duplex stability when compared with full RNA duplexes.No substantial increase in stability towards snake venom phosphodiesterase (SVPD) was observed.