(2R,3S,5R)-2-((Bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-5-(4-(2-(4-(tert-butyl)phenoxy)acetamido)-2-oxopyrimidin-1(2H)-yl)tetrahydrofuran-3-yl (2-cyanoethyl) diiSopropylphosphoramidite

95%

Reagent Code: #229801
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CAS Number 149989-59-3

science Other reagents with same CAS 149989-59-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 920.04 g/mol
Formula C₅₁H₆₂N₅O₉P
badge Registry Numbers
MDL Number MFCD01941140
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used in the solid-phase synthesis of oligonucleotides, particularly in the preparation of modified RNA strands for research and therapeutic applications. Its phosphoramidite group enables efficient coupling during automated synthesis, while the protecting groups ensure high yield and specificity. Commonly applied in the development of antisense oligonucleotides, siRNA, and other nucleic acid-based drugs where precise modification is required for stability and biological activity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿3,280.00
(2R,3S,5R)-2-((Bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-5-(4-(2-(4-(tert-butyl)phenoxy)acetamido)-2-oxopyrimidin-1(2H)-yl)tetrahydrofuran-3-yl (2-cyanoethyl) diiSopropylphosphoramidite
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Used in the solid-phase synthesis of oligonucleotides, particularly in the preparation of modified RNA strands for research and therapeutic applications. Its phosphoramidite group enables efficient coupling during automated synthesis, while the protecting groups ensure high yield and specificity. Commonly applied in the development of antisense oligonucleotides, siRNA, and other nucleic acid-based drugs where precise modification is required for stability and biological activity.

Used in the solid-phase synthesis of oligonucleotides, particularly in the preparation of modified RNA strands for research and therapeutic applications. Its phosphoramidite group enables efficient coupling during automated synthesis, while the protecting groups ensure high yield and specificity. Commonly applied in the development of antisense oligonucleotides, siRNA, and other nucleic acid-based drugs where precise modification is required for stability and biological activity.

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