N2-Isobutyryl-3',5'-O-(1,1,3,3-tetraisopropyl-1,3-disiloxanediyl)guanosine

95%

Reagent Code: #97169
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CAS Number 87865-78-9

science Other reagents with same CAS 87865-78-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 595.84 g/mol
Formula C₂₆H₄₅N₅O₇Si₂
badge Registry Numbers
MDL Number MFCD15145300
inventory_2 Storage & Handling
Density 1.31±0.1 g/cm3(Predicted)
Storage 2-8℃

description Product Description

This chemical is primarily used in the synthesis of modified nucleosides, which are essential in the development of oligonucleotides for research and therapeutic applications. It serves as a protected guanosine derivative, enabling precise control over chemical reactions during the construction of nucleic acid sequences. This is particularly valuable in the production of antisense oligonucleotides, siRNA, and other gene-silencing technologies. The protective groups, such as the tetraisopropyldisiloxane moiety, ensure stability and selectivity during synthetic processes, making it a crucial intermediate in medicinal chemistry and molecular biology research. Its application is also significant in the study of RNA structure and function, as well as in the development of nucleotide-based drugs for treating genetic disorders and viral infections.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿12,285.00
inventory 1g
10-20 days ฿3,654.00

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N2-Isobutyryl-3',5'-O-(1,1,3,3-tetraisopropyl-1,3-disiloxanediyl)guanosine
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This chemical is primarily used in the synthesis of modified nucleosides, which are essential in the development of oligonucleotides for research and therapeutic applications. It serves as a protected guanosine derivative, enabling precise control over chemical reactions during the construction of nucleic acid sequences. This is particularly valuable in the production of antisense oligonucleotides, siRNA, and other gene-silencing technologies. The protective groups, such as the tetraisopropyldisiloxane m

This chemical is primarily used in the synthesis of modified nucleosides, which are essential in the development of oligonucleotides for research and therapeutic applications. It serves as a protected guanosine derivative, enabling precise control over chemical reactions during the construction of nucleic acid sequences. This is particularly valuable in the production of antisense oligonucleotides, siRNA, and other gene-silencing technologies. The protective groups, such as the tetraisopropyldisiloxane moiety, ensure stability and selectivity during synthetic processes, making it a crucial intermediate in medicinal chemistry and molecular biology research. Its application is also significant in the study of RNA structure and function, as well as in the development of nucleotide-based drugs for treating genetic disorders and viral infections.

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