Ethyl 2,6-dichloro-9H-purine-9-acetate

95%

Reagent Code: #184537
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CAS Number 171827-50-2

science Other reagents with same CAS 171827-50-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 275.09 g/mol
Formula C₉H₈Cl₂N₄O₂
badge Registry Numbers
MDL Number MFCD30471974
thermostat Physical Properties
Melting Point 112-114 °C
Boiling Point 387.8±52.0 °C(Predicted)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of purine-based drugs. It plays a role in creating analogs with potential antiviral, anticancer, or immunosuppressive activity. The 2- and 6-chloro groups and the ester functional group allow for selective modifications, such as nucleophilic substitutions with amino or hydroxy groups, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in research settings to develop nucleoside derivatives and kinase inhibitors.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,400.00
inventory 250mg
10-20 days ฿18,200.00
inventory 1g
10-20 days ฿43,680.00
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Ethyl 2,6-dichloro-9H-purine-9-acetate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of purine-based drugs. It plays a role in creating analogs with potential antiviral, anticancer, or immunosuppressive activity. The 2- and 6-chloro groups and the ester functional group allow for selective modifications, such as nucleophilic substitutions with amino or hydroxy groups, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in research settin

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of purine-based drugs. It plays a role in creating analogs with potential antiviral, anticancer, or immunosuppressive activity. The 2- and 6-chloro groups and the ester functional group allow for selective modifications, such as nucleophilic substitutions with amino or hydroxy groups, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in research settings to develop nucleoside derivatives and kinase inhibitors.

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