2'-O-tert-Butyldimethylsilyl-N6-Benzoyl-adenosine

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Reagent Code: #40422
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CAS Number 69504-07-0

science Other reagents with same CAS 69504-07-0

blur_circular Chemical Specifications

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Weight 485.61 g/mol
Formula C₂₃H₃₁N₅O₅Si
badge Registry Numbers
MDL Number MFCD28134644
inventory_2 Storage & Handling
Density 1.33±0.1 g/cm3(Predicted)
Storage 2-8℃

description Product Description

This chemical is primarily utilized in the synthesis and modification of nucleosides, which are crucial building blocks in the development of oligonucleotides and RNA analogs. Its protective groups, the tert-butyldimethylsilyl (TBDMS) and benzoyl moieties, are strategically employed to shield specific reactive sites during chemical reactions, ensuring selective and controlled synthesis. This compound is particularly valuable in the production of modified RNA molecules for research in molecular biology, drug development, and therapeutic applications, such as antisense oligonucleotides and siRNA. Its role in enabling precise nucleotide modifications makes it a key reagent in the study of gene expression and the development of targeted therapies.

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inventory 1g
10-20 days ฿57,897.00

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2'-O-tert-Butyldimethylsilyl-N6-Benzoyl-adenosine
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This chemical is primarily utilized in the synthesis and modification of nucleosides, which are crucial building blocks in the development of oligonucleotides and RNA analogs. Its protective groups, the tert-butyldimethylsilyl (TBDMS) and benzoyl moieties, are strategically employed to shield specific reactive sites during chemical reactions, ensuring selective and controlled synthesis. This compound is particularly valuable in the production of modified RNA molecules for research in molecular biology, d

This chemical is primarily utilized in the synthesis and modification of nucleosides, which are crucial building blocks in the development of oligonucleotides and RNA analogs. Its protective groups, the tert-butyldimethylsilyl (TBDMS) and benzoyl moieties, are strategically employed to shield specific reactive sites during chemical reactions, ensuring selective and controlled synthesis. This compound is particularly valuable in the production of modified RNA molecules for research in molecular biology, drug development, and therapeutic applications, such as antisense oligonucleotides and siRNA. Its role in enabling precise nucleotide modifications makes it a key reagent in the study of gene expression and the development of targeted therapies.

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