N4-Acetyl-3'-O-tert-butyldimethylsilyl-5'-O-DMT-cytidine

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Reagent Code: #97279
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CAS Number 123956-65-0

science Other reagents with same CAS 123956-65-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 701.88 g/mol
Formula C₃₈H₄₇N₃O₈Si
badge Registry Numbers
MDL Number MFCD22124263
inventory_2 Storage & Handling
Density 1.19±0.1 g/cm3(Predicted)
Storage 2-8°C

description Product Description

This compound is primarily used in the synthesis of oligonucleotides, particularly in the field of nucleic acid chemistry. It serves as a protected nucleoside intermediate, ensuring selective reactivity during the construction of DNA or RNA sequences. The tert-butyldimethylsilyl (TBDMS) group protects the 3'-hydroxyl, while the dimethoxytrityl (DMT) group safeguards the 5'-hydroxyl, allowing for controlled stepwise assembly in solid-phase synthesis. The acetyl group on the N4 position of cytidine prevents unwanted side reactions during the process. This compound is essential in producing high-purity oligonucleotides for applications such as gene synthesis, PCR primers, and antisense therapeutics. Its use is critical in research and development of genetic engineering, molecular diagnostics, and therapeutic oligonucleotides.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿14,940.00
inventory 250mg
10-20 days ฿5,220.00

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N4-Acetyl-3'-O-tert-butyldimethylsilyl-5'-O-DMT-cytidine
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This compound is primarily used in the synthesis of oligonucleotides, particularly in the field of nucleic acid chemistry. It serves as a protected nucleoside intermediate, ensuring selective reactivity during the construction of DNA or RNA sequences. The tert-butyldimethylsilyl (TBDMS) group protects the 3'-hydroxyl, while the dimethoxytrityl (DMT) group safeguards the 5'-hydroxyl, allowing for controlled stepwise assembly in solid-phase synthesis. The acetyl group on the N4 position of cytidine prevent

This compound is primarily used in the synthesis of oligonucleotides, particularly in the field of nucleic acid chemistry. It serves as a protected nucleoside intermediate, ensuring selective reactivity during the construction of DNA or RNA sequences. The tert-butyldimethylsilyl (TBDMS) group protects the 3'-hydroxyl, while the dimethoxytrityl (DMT) group safeguards the 5'-hydroxyl, allowing for controlled stepwise assembly in solid-phase synthesis. The acetyl group on the N4 position of cytidine prevents unwanted side reactions during the process. This compound is essential in producing high-purity oligonucleotides for applications such as gene synthesis, PCR primers, and antisense therapeutics. Its use is critical in research and development of genetic engineering, molecular diagnostics, and therapeutic oligonucleotides.

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