5'-O-DMT-5-iodo-2'-deoxyuridine

97%

Reagent Code: #58371
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CAS Number 104375-88-4

science Other reagents with same CAS 104375-88-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 656.46 g/mol
Formula C₃₀H₂₉IN₂O₇
badge Registry Numbers
MDL Number MFCD01631069
thermostat Physical Properties
Melting Point >128 °C (decomp)
inventory_2 Storage & Handling
Density 1.60±0.1 g/cm3(Predicted)
Storage 2-8℃

description Product Description

This chemical is primarily used in the field of nucleic acid research and drug development. It serves as a protected nucleoside derivative, enabling the synthesis of modified oligonucleotides. The 5'-O-DMT group acts as a protecting group during solid-phase oligonucleotide synthesis, ensuring selective reactions at other sites. The 5-iodo modification allows for further functionalization or cross-linking in the development of therapeutic agents, particularly in antiviral and anticancer research. It is also utilized in radiolabeling studies for tracking and imaging purposes in biological systems. Its applications extend to the study of DNA repair mechanisms and the development of targeted therapies.

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inventory 5g
10-20 days ฿12,816.00

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5'-O-DMT-5-iodo-2'-deoxyuridine
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This chemical is primarily used in the field of nucleic acid research and drug development. It serves as a protected nucleoside derivative, enabling the synthesis of modified oligonucleotides. The 5'-O-DMT group acts as a protecting group during solid-phase oligonucleotide synthesis, ensuring selective reactions at other sites. The 5-iodo modification allows for further functionalization or cross-linking in the development of therapeutic agents, particularly in antiviral and anticancer research. It is al

This chemical is primarily used in the field of nucleic acid research and drug development. It serves as a protected nucleoside derivative, enabling the synthesis of modified oligonucleotides. The 5'-O-DMT group acts as a protecting group during solid-phase oligonucleotide synthesis, ensuring selective reactions at other sites. The 5-iodo modification allows for further functionalization or cross-linking in the development of therapeutic agents, particularly in antiviral and anticancer research. It is also utilized in radiolabeling studies for tracking and imaging purposes in biological systems. Its applications extend to the study of DNA repair mechanisms and the development of targeted therapies.

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