N-Acetyl-3',5'-O-(1,1,3,3-tetraisopropyl-1,3-disiloxanediyl)adenosine

95%

Reagent Code: #43840
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CAS Number 828247-65-0

science Other reagents with same CAS 828247-65-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 551.78 g/mol
Formula C₂₄H₄₁N₅O₆Si₂
badge Registry Numbers
MDL Number MFCD28016486
inventory_2 Storage & Handling
Density 1.29±0.1 g/cm3(Predicted)
Storage 2-8℃

description Product Description

This compound is primarily utilized in the synthesis of modified nucleosides and nucleotides, playing a crucial role in the development of oligonucleotides for research and therapeutic applications. It serves as a protected intermediate in organic synthesis, particularly in the preparation of RNA analogs, where the tetraisopropyldisiloxane (TIPDS) group safeguards the 3' and 5' hydroxyl positions during chemical reactions. This protection allows for selective modification of the adenosine molecule, enabling the creation of specialized nucleosides used in studies involving gene expression, antisense technology, and the development of antiviral or anticancer agents. Its application is significant in the field of medicinal chemistry and biochemistry for designing molecules with enhanced stability and specificity.

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inventory 25g
10-20 days ฿37,818.00

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N-Acetyl-3',5'-O-(1,1,3,3-tetraisopropyl-1,3-disiloxanediyl)adenosine
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This compound is primarily utilized in the synthesis of modified nucleosides and nucleotides, playing a crucial role in the development of oligonucleotides for research and therapeutic applications. It serves as a protected intermediate in organic synthesis, particularly in the preparation of RNA analogs, where the tetraisopropyldisiloxane (TIPDS) group safeguards the 3' and 5' hydroxyl positions during chemical reactions. This protection allows for selective modification of the adenosine molecule, enabl

This compound is primarily utilized in the synthesis of modified nucleosides and nucleotides, playing a crucial role in the development of oligonucleotides for research and therapeutic applications. It serves as a protected intermediate in organic synthesis, particularly in the preparation of RNA analogs, where the tetraisopropyldisiloxane (TIPDS) group safeguards the 3' and 5' hydroxyl positions during chemical reactions. This protection allows for selective modification of the adenosine molecule, enabling the creation of specialized nucleosides used in studies involving gene expression, antisense technology, and the development of antiviral or anticancer agents. Its application is significant in the field of medicinal chemistry and biochemistry for designing molecules with enhanced stability and specificity.

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