3'-Chloro-3'-Deoxythymidine

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Reagent Code: #157026
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CAS Number 25526-94-7

science Other reagents with same CAS 25526-94-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 260.67 g/mol
Formula C₁₀H₁₃ClN₂O₄
badge Registry Numbers
MDL Number MFCD22418073
thermostat Physical Properties
Melting Point 180-182 °C
inventory_2 Storage & Handling
Density 1.48±0.1 g/cm3(Predicted)
Storage -20°C, Sealed

description Product Description

Used in research as a modified nucleoside for studying DNA synthesis and polymerase mechanisms. Acts as a chain terminator in some enzymatic reactions, making it valuable in molecular biology techniques that require controlled DNA elongation. Also explored for potential antiviral properties due to its structural similarity to thymidine analogs known to interfere with viral replication. Its chloro modification enhances stability and alters substrate recognition in certain enzyme systems, useful in biochemical assays and drug development studies.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿42,520.00
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3'-Chloro-3'-Deoxythymidine
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Used in research as a modified nucleoside for studying DNA synthesis and polymerase mechanisms. Acts as a chain terminator in some enzymatic reactions, making it valuable in molecular biology techniques that require controlled DNA elongation. Also explored for potential antiviral properties due to its structural similarity to thymidine analogs known to interfere with viral replication. Its chloro modification enhances stability and alters substrate recognition in certain enzyme systems, useful in biochem

Used in research as a modified nucleoside for studying DNA synthesis and polymerase mechanisms. Acts as a chain terminator in some enzymatic reactions, making it valuable in molecular biology techniques that require controlled DNA elongation. Also explored for potential antiviral properties due to its structural similarity to thymidine analogs known to interfere with viral replication. Its chloro modification enhances stability and alters substrate recognition in certain enzyme systems, useful in biochemical assays and drug development studies.

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