2,6-Dichloro-9-isopropyl-9H-purine

97%

Reagent Code: #178184
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CAS Number 203436-45-7

science Other reagents with same CAS 203436-45-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 231.08 g/mol
Formula C₈H₈Cl₂N₄
badge Registry Numbers
MDL Number MFCD11047295
thermostat Physical Properties
Melting Point 150-151 °C
Boiling Point 315.1±52.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.58±0.1 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in the development of kinase inhibitors for cancer therapy. It serves as a building block in medicinal chemistry for modifying purine scaffolds to enhance selectivity and potency in drug candidates. Also employed in research settings to study cell signaling pathways and enzyme regulation. Its halogenated structure allows for further functionalization via cross-coupling reactions, making it valuable in the design of novel pharmaceuticals.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,570.00
inventory 5g
10-20 days ฿11,410.00

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2,6-Dichloro-9-isopropyl-9H-purine
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Used as a key intermediate in the synthesis of biologically active compounds, particularly in the development of kinase inhibitors for cancer therapy. It serves as a building block in medicinal chemistry for modifying purine scaffolds to enhance selectivity and potency in drug candidates. Also employed in research settings to study cell signaling pathways and enzyme regulation. Its halogenated structure allows for further functionalization via cross-coupling reactions, making it valuable in the design of

Used as a key intermediate in the synthesis of biologically active compounds, particularly in the development of kinase inhibitors for cancer therapy. It serves as a building block in medicinal chemistry for modifying purine scaffolds to enhance selectivity and potency in drug candidates. Also employed in research settings to study cell signaling pathways and enzyme regulation. Its halogenated structure allows for further functionalization via cross-coupling reactions, making it valuable in the design of novel pharmaceuticals.

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