2'-Deoxy-5'-O-DMT-5-iodouridine 3'-CE phosphoramidite

≥95%

Reagent Code: #180466
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CAS Number 178925-48-9

science Other reagents with same CAS 178925-48-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 856.7 g/mol
Formula C₃₉H₄₆IN₄O₈P
badge Registry Numbers
MDL Number MFCD00080319
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Widely used in oligonucleotide synthesis, this compound enables the site-specific incorporation of 5-iodouridine into DNA strands. The iodine moiety acts as a handle for further functionalization, such as coupling via palladium-catalyzed cross-coupling reactions, allowing the attachment of labels, probes, or other functional groups. Its DMT and CE phosphoramidite protecting groups ensure compatibility with standard solid-phase synthesis protocols, making it ideal for automated DNA synthesizers. It is particularly valuable in the development of modified antisense oligonucleotides, diagnostic probes, and nucleic acid-based therapeutics where precise modification is required. The presence of the iodine atom also facilitates structural studies using techniques like X-ray crystallography or as a radiosensitizer in photodynamic therapy research.

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inventory 250mg
10-20 days ฿22,790.00

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2'-Deoxy-5'-O-DMT-5-iodouridine 3'-CE phosphoramidite
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Widely used in oligonucleotide synthesis, this compound enables the site-specific incorporation of 5-iodouridine into DNA strands. The iodine moiety acts as a handle for further functionalization, such as coupling via palladium-catalyzed cross-coupling reactions, allowing the attachment of labels, probes, or other functional groups. Its DMT and CE phosphoramidite protecting groups ensure compatibility with standard solid-phase synthesis protocols, making it ideal for automated DNA synthesizers. It is par

Widely used in oligonucleotide synthesis, this compound enables the site-specific incorporation of 5-iodouridine into DNA strands. The iodine moiety acts as a handle for further functionalization, such as coupling via palladium-catalyzed cross-coupling reactions, allowing the attachment of labels, probes, or other functional groups. Its DMT and CE phosphoramidite protecting groups ensure compatibility with standard solid-phase synthesis protocols, making it ideal for automated DNA synthesizers. It is particularly valuable in the development of modified antisense oligonucleotides, diagnostic probes, and nucleic acid-based therapeutics where precise modification is required. The presence of the iodine atom also facilitates structural studies using techniques like X-ray crystallography or as a radiosensitizer in photodynamic therapy research.

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