3′, 5′-Di-O-acetyl-5-bromo-2′-deoxyuridine

95%

Reagent Code: #178326
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CAS Number 6161-23-5

science Other reagents with same CAS 6161-23-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 391.17 g/mol
Formula C₁₃H₁₅BrN₂O₇
badge Registry Numbers
MDL Number MFCD00057407
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in the synthesis of antiviral and anticancer agents, this compound plays a key role in modifying nucleoside structures to enhance biological activity. The acetyl groups protect hydroxyl functionalities during synthesis, allowing selective reactions at other sites. The bromine atom serves as a handle for further chemical modifications, such as coupling reactions in the preparation of nucleoside analogs. It is particularly valuable in the development of prodrugs and in studying DNA incorporation mechanisms in rapidly dividing cells. Its derivatives are explored for activity against viruses like herpes simplex and certain tumor cell lines.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,460.00
inventory 1g
10-20 days ฿9,330.00
inventory 5g
10-20 days ฿33,660.00

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3′, 5′-Di-O-acetyl-5-bromo-2′-deoxyuridine
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Used primarily as an intermediate in the synthesis of antiviral and anticancer agents, this compound plays a key role in modifying nucleoside structures to enhance biological activity. The acetyl groups protect hydroxyl functionalities during synthesis, allowing selective reactions at other sites. The bromine atom serves as a handle for further chemical modifications, such as coupling reactions in the preparation of nucleoside analogs. It is particularly valuable in the development of prodrugs and in stu

Used primarily as an intermediate in the synthesis of antiviral and anticancer agents, this compound plays a key role in modifying nucleoside structures to enhance biological activity. The acetyl groups protect hydroxyl functionalities during synthesis, allowing selective reactions at other sites. The bromine atom serves as a handle for further chemical modifications, such as coupling reactions in the preparation of nucleoside analogs. It is particularly valuable in the development of prodrugs and in studying DNA incorporation mechanisms in rapidly dividing cells. Its derivatives are explored for activity against viruses like herpes simplex and certain tumor cell lines.

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