147490-71-9

Basic information

• Product Name: 2'-O-<1-(2-fluorophenyl)-4-methoxypiperidin-4-yl>-6-N-pivaloyladenosine
• Synonyms: 2'-O-<1-(2-fluorophenyl)-4-methoxypiperidin-4-yl>-6-N-pivaloyladenosine
• CAS NO: 147490-71-9
• Molecular Weight: 558.61
• Mol File: 147490-71-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2'-O-<1-(2-fluorophenyl)-4-methoxypiperidin-4-yl>-6-N-pivaloyladenosine(CAS DataBase Reference)
• NIST Chemistry Reference: 2'-O-<1-(2-fluorophenyl)-4-methoxypiperidin-4-yl>-6-N-pivaloyladenosine(147490-71-9)
• EPA Substance Registry System: 2'-O-<1-(2-fluorophenyl)-4-methoxypiperidin-4-yl>-6-N-pivaloyladenosine(147490-71-9)

Safety Data

• Hazardous Substances Data: 147490-71-9(Hazardous Substances Data)

Upstream product

• 58-61-7 adenosine 
• 147490-69-5 6-N-pivaloyl-adenosine 
• 3282-30-2 pivaloyl chloride 
• 1053643-25-6 2,2-Dimethyl-N-[9-((2R,3R,3aR,9aR)-5,5,7,7-tetraisopropyl-3-trimethylsilanyloxy-tetrahydro-1,4,6,8-tetraoxa-5,7-disila-cyclopentacycloocten-2-yl)-9H-purin-6-yl]-propionamide 
• 142741-95-5 3',5'-O-(1,1,3,3-Tetraisopropyldisiloxane-1,3-diyl)-6-N-pivaloyladenosine 
• 115012-52-7 1-(2-Fluorophenyl)-4-methoxy-1,2,5,6-tetrahydropyridine 
• 69304-45-6 3',5'-O-(1,1,3,3-tetra-isopropyldisiloxane-1,3-diyl)adenosine 
• 160905-59-9 2'-O-<1-(2-fluorophenyl)-4-methoxypiperidin-4-yl>-6-N-pivaloyl-3',5'-O-(tetraisopropyldisiloxane-1,3-diyl)adenosine 

Downstream Products

• 147490-74-2 2'-O-<1-(2-fluorophenyl)-4-methoxypiperidin-4-yl>-5'-O-(9-phenylxanthen-9-yl)-6-N-pivaloyladenosine 
• 160905-64-6 5'-O-(tert-butyldiphenylsilyl)-2'-O-<1-(2-fluorophenyl)-4-methoxypiperidin-4-yl>-3'-O-(9-phenylxanthen-9-yl)-6-N-pivaloyladenosine 
• 115012-46-9 1-(2-fluorophenyl)piperidin-4-one 
• 147490-69-5 6-N-pivaloyl-adenosine 
• 160905-67-9 5'-O-(tert-butyldiphenylsilyl)-2'-O-<1-(2-fluorophenyl)-4-methoxypiperidin-4-yl>-6-N-pivaloyladenosine 

Relevant articles and documents

Novel Solid-phase Synthesis of Branched Oligoribonucleotides, including a Substrate for the RNA Debranching Enzyme

An effective new route for synthesizing branched oligoribionucleotides in the solid phase in the 5' to 3' direction has been developed.This required the synthesis of reversed monomers, viz. protected nucleoside 5'-phosphoramidites bearing 2'-O-Fpmp and 3'