N4-Benzoyl-5'-O-tert-butyldimethylsilyl-2'-deoxycytidine

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Reagent Code: #52950
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CAS Number 51549-36-1

science Other reagents with same CAS 51549-36-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 445.58 g/mol
Formula C₂₂H₃₁N₃O₅Si
badge Registry Numbers
MDL Number MFCD04972284
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

N4-Benzoyl-5'-O-tert-butyldimethylsilyl-2'-deoxycytidine is primarily used in the synthesis of modified nucleosides and nucleotides. It serves as a key intermediate in the preparation of oligonucleotides, which are essential for research in molecular biology and genetic engineering. The tert-butyldimethylsilyl (TBDMS) group protects the 5'-hydroxyl during chemical reactions, ensuring selective modification of other functional groups. The benzoyl group at the N4 position stabilizes the cytidine base, preventing unwanted side reactions. This compound is particularly valuable in the automated synthesis of DNA sequences, enabling the production of custom oligonucleotides for applications such as PCR, gene editing, and antisense therapy. Its use ensures high yield and purity in the construction of complex nucleic acid structures.

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Test Parameter Specification
Appearance White Solid
Purity 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,880.00
inventory 50mg
10-20 days ฿1,350.00
inventory 1g
10-20 days ฿15,000.00

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N4-Benzoyl-5'-O-tert-butyldimethylsilyl-2'-deoxycytidine
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N4-Benzoyl-5'-O-tert-butyldimethylsilyl-2'-deoxycytidine is primarily used in the synthesis of modified nucleosides and nucleotides. It serves as a key intermediate in the preparation of oligonucleotides, which are essential for research in molecular biology and genetic engineering. The tert-butyldimethylsilyl (TBDMS) group protects the 5'-hydroxyl during chemical reactions, ensuring selective modification of other functional groups. The benzoyl group at the N4 position stabilizes the cytidine base, preventing unwanted side reactions. This compound is particularly valuable in the automated synthesis of DNA sequences, enabling the production of custom oligonucleotides for applications such as PCR, gene editing, and antisense therapy. Its use ensures high yield and purity in the construction of complex nucleic acid structures.
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