1-((4aR,6R,7R,7aS)-2,2-Di-tert-butyl-7-hydroxytetrahydro-4H-furo[3,2-d][1,3,2]dioxasilin-6-yl)pyrimidine-2,4(1H,3H)-dione

98%

Reagent Code: #229374
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CAS Number 97219-04-0

science Other reagents with same CAS 97219-04-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 384.5 g/mol
Formula C₁₇H₂₈N₂O₆Si
inventory_2 Storage & Handling
Density 1.24±0.1 g/cm3(Predicted)
Storage -20°C, Sealed, Dry

description Product Description

Used in organic synthesis as a protected nucleoside intermediate, particularly in the preparation of modified RNA or DNA analogs. The compound's silyl-protected structure stabilizes the sugar moiety during phosphoramidite-based oligonucleotide assembly, making it valuable in antisense technology and therapeutic oligonucleotide development. Its steric bulk helps reduce side reactions during coupling steps in solid-phase synthesis. Also employed in the study of nucleic acid enzymes due to its resistance to premature deprotection under mild acidic conditions.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,430.00
inventory 5g
10-20 days ฿12,990.00

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1-((4aR,6R,7R,7aS)-2,2-Di-tert-butyl-7-hydroxytetrahydro-4H-furo[3,2-d][1,3,2]dioxasilin-6-yl)pyrimidine-2,4(1H,3H)-dione
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Used in organic synthesis as a protected nucleoside intermediate, particularly in the preparation of modified RNA or DNA analogs. The compound's silyl-protected structure stabilizes the sugar moiety during phosphoramidite-based oligonucleotide assembly, making it valuable in antisense technology and therapeutic oligonucleotide development. Its steric bulk helps reduce side reactions during coupling steps in solid-phase synthesis. Also employed in the study of nucleic acid enzymes due to its resistance to

Used in organic synthesis as a protected nucleoside intermediate, particularly in the preparation of modified RNA or DNA analogs. The compound's silyl-protected structure stabilizes the sugar moiety during phosphoramidite-based oligonucleotide assembly, making it valuable in antisense technology and therapeutic oligonucleotide development. Its steric bulk helps reduce side reactions during coupling steps in solid-phase synthesis. Also employed in the study of nucleic acid enzymes due to its resistance to premature deprotection under mild acidic conditions.

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