5'-O-DMT-2'-O-TBDMS-Bz-rC

98%

Reagent Code: #222217
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CAS Number 81256-87-3

science Other reagents with same CAS 81256-87-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 763.963 g/mol
Formula C₄₃H₄₉N₃O₈Si
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used in solid-phase oligonucleotide synthesis, particularly for the preparation of RNA strands. The DMT (dimethoxytrityl) group protects the 5'-hydroxyl during chain assembly, allowing stepwise addition of nucleotides and enabling monitoring of coupling efficiency through trityl cation release. The TBDMS (tert-butyldimethylsilyl) group selectively protects the 2'-hydroxyl, providing stability and regioselectivity during synthesis while being removable under mild conditions post-assembly. The benzoyl (Bz) group protects the cytosine base, minimizing side reactions. This modified nucleoside is essential for producing high-purity RNA for research, diagnostics, and therapeutic applications such as antisense oligonucleotides, siRNA, and CRISPR guide RNAs.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿2,000.00
inventory 100mg
10-20 days ฿5,000.00

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5'-O-DMT-2'-O-TBDMS-Bz-rC
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Used in solid-phase oligonucleotide synthesis, particularly for the preparation of RNA strands. The DMT (dimethoxytrityl) group protects the 5'-hydroxyl during chain assembly, allowing stepwise addition of nucleotides and enabling monitoring of coupling efficiency through trityl cation release. The TBDMS (tert-butyldimethylsilyl) group selectively protects the 2'-hydroxyl, providing stability and regioselectivity during synthesis while being removable under mild conditions post-assembly. The benzoyl (Bz)

Used in solid-phase oligonucleotide synthesis, particularly for the preparation of RNA strands. The DMT (dimethoxytrityl) group protects the 5'-hydroxyl during chain assembly, allowing stepwise addition of nucleotides and enabling monitoring of coupling efficiency through trityl cation release. The TBDMS (tert-butyldimethylsilyl) group selectively protects the 2'-hydroxyl, providing stability and regioselectivity during synthesis while being removable under mild conditions post-assembly. The benzoyl (Bz) group protects the cytosine base, minimizing side reactions. This modified nucleoside is essential for producing high-purity RNA for research, diagnostics, and therapeutic applications such as antisense oligonucleotides, siRNA, and CRISPR guide RNAs.

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