2-Chloro-6-O-methyl-inosine

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Reagent Code: #42976
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CAS Number 15465-92-6

science Other reagents with same CAS 15465-92-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 316.69772 g/mol
Formula C₁₁H₁₃ClN₄O₅
thermostat Physical Properties
Melting Point 140 °C(Solv: isopropanol (67-63-0))
Boiling Point 587.8±60.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.95±0.1 g/cm3(Predicted)
Storage 2-8°C, stored in inert gas

description Product Description

Used primarily in biochemical research, this compound serves as a modified nucleoside to study RNA structure and function. It aids in understanding the role of methylation and chlorination in nucleic acids, particularly in the context of RNA modifications and their impact on gene expression. Additionally, it is employed in the synthesis of antiviral and anticancer agents, where its structural modifications can enhance drug efficacy and specificity. Researchers also utilize it to explore enzyme mechanisms, particularly those involving nucleoside kinases and phosphorylases, contributing to advancements in enzymology and drug development.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,563.00
inventory 250mg
10-20 days ฿1,692.00

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2-Chloro-6-O-methyl-inosine
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Used primarily in biochemical research, this compound serves as a modified nucleoside to study RNA structure and function. It aids in understanding the role of methylation and chlorination in nucleic acids, particularly in the context of RNA modifications and their impact on gene expression. Additionally, it is employed in the synthesis of antiviral and anticancer agents, where its structural modifications can enhance drug efficacy and specificity. Researchers also utilize it to explore enzyme mechanisms

Used primarily in biochemical research, this compound serves as a modified nucleoside to study RNA structure and function. It aids in understanding the role of methylation and chlorination in nucleic acids, particularly in the context of RNA modifications and their impact on gene expression. Additionally, it is employed in the synthesis of antiviral and anticancer agents, where its structural modifications can enhance drug efficacy and specificity. Researchers also utilize it to explore enzyme mechanisms, particularly those involving nucleoside kinases and phosphorylases, contributing to advancements in enzymology and drug development.

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