1-((2R,3R,4R,5R)-4-((tert-Butyldimethylsilyl)oxy)-5-(((tert-butyldimethylsilyl)oxy)methyl)-3-methoxytetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione

95%

Reagent Code: #231424
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CAS Number 367511-37-3

science Other reagents with same CAS 367511-37-3

blur_circular Chemical Specifications

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Weight 486.75 g/mol
Formula C₂₂H₄₂N₂O₆Si₂
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a protected nucleoside intermediate in the synthesis of antiviral and anticancer agents, particularly in the preparation of modified RNA or DNA analogs. The silyl protecting groups allow selective manipulation of hydroxyl functionalities during oligonucleotide assembly, making it valuable in pharmaceutical research and development of nucleoside-based therapeutics. Commonly employed in solid-phase synthesis and used to enhance stability and solubility during multi-step reactions.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,600.00
inventory 1g
10-20 days ฿4,310.00
inventory 5g
10-20 days ฿16,330.00

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1-((2R,3R,4R,5R)-4-((tert-Butyldimethylsilyl)oxy)-5-(((tert-butyldimethylsilyl)oxy)methyl)-3-methoxytetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione
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Used as a protected nucleoside intermediate in the synthesis of antiviral and anticancer agents, particularly in the preparation of modified RNA or DNA analogs. The silyl protecting groups allow selective manipulation of hydroxyl functionalities during oligonucleotide assembly, making it valuable in pharmaceutical research and development of nucleoside-based therapeutics. Commonly employed in solid-phase synthesis and used to enhance stability and solubility during multi-step reactions.

Used as a protected nucleoside intermediate in the synthesis of antiviral and anticancer agents, particularly in the preparation of modified RNA or DNA analogs. The silyl protecting groups allow selective manipulation of hydroxyl functionalities during oligonucleotide assembly, making it valuable in pharmaceutical research and development of nucleoside-based therapeutics. Commonly employed in solid-phase synthesis and used to enhance stability and solubility during multi-step reactions.

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