(1R,3R,4R,7S)-3-(4-Benzamido-5-methyl-2-oxopyrimidin-1(2H)-yl)-1-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-2,5-dioxabicyclo[2.2.1]heptan-7-yl(2-cyanoethyl)diisopropylphosphoramidite

99%

Reagent Code: #231812
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CAS Number 206055-82-5

science Other reagents with same CAS 206055-82-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 875.94 g/mol
Formula C₄₈H₅₄N₅O₉P
inventory_2 Storage & Handling
Storage -20°C, Sealed, Drying, Inert Gas

description Product Description

Used in solid-phase oligonucleotide synthesis as a phosphoramidite building block for introducing modified nucleosides into DNA or RNA strands. The compound enables site-specific incorporation of a pyrimidine derivative with a benzamido group, useful in antisense technology, diagnostic probes, and therapeutic oligonucleotides. The protecting groups ensure compatibility with automated synthesis, while the diisopropylphosphoramidite moiety allows for efficient coupling. The 2-cyanoethyl group facilitates later deprotection under mild basic conditions. Commonly applied in research settings for developing nucleic acid-based drugs and functional genomics tools.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,400.00
inventory 250mg
10-20 days ฿6,010.00

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(1R,3R,4R,7S)-3-(4-Benzamido-5-methyl-2-oxopyrimidin-1(2H)-yl)-1-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-2,5-dioxabicyclo[2.2.1]heptan-7-yl(2-cyanoethyl)diisopropylphosphoramidite
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Used in solid-phase oligonucleotide synthesis as a phosphoramidite building block for introducing modified nucleosides into DNA or RNA strands. The compound enables site-specific incorporation of a pyrimidine derivative with a benzamido group, useful in antisense technology, diagnostic probes, and therapeutic oligonucleotides. The protecting groups ensure compatibility with automated synthesis, while the diisopropylphosphoramidite moiety allows for efficient coupling. The 2-cyanoethyl group facilitates l

Used in solid-phase oligonucleotide synthesis as a phosphoramidite building block for introducing modified nucleosides into DNA or RNA strands. The compound enables site-specific incorporation of a pyrimidine derivative with a benzamido group, useful in antisense technology, diagnostic probes, and therapeutic oligonucleotides. The protecting groups ensure compatibility with automated synthesis, while the diisopropylphosphoramidite moiety allows for efficient coupling. The 2-cyanoethyl group facilitates later deprotection under mild basic conditions. Commonly applied in research settings for developing nucleic acid-based drugs and functional genomics tools.

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