6-Chloro-3-iodoimidazo[1,2-b]pyridazine

≥96%

Reagent Code: #161813
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CAS Number 923595-49-7

science Other reagents with same CAS 923595-49-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 279.47 g/mol
Formula C₆H₃ClIN₃
badge Registry Numbers
EC Number 200-001-2
MDL Number MFCD11044749
inventory_2 Storage & Handling
Density 2.34/cm³
Storage 2-8°C, dry, sealed

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly for targeting tyrosine kinases involved in cancer cell proliferation. Its halogenated structure allows for selective cross-coupling reactions, enabling the development of novel drug candidates. Also employed in the study of structure-activity relationships (SAR) within imidazopyridazine-based compounds to optimize biological activity and metabolic stability.

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Test Parameter Specification
Appearance Solid
Purity (%) 96-100%
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿357.50
inventory 1g
10-20 days ฿1,023.00
inventory 5g
10-20 days ฿3,437.50

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6-Chloro-3-iodoimidazo[1,2-b]pyridazine
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Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly for targeting tyrosine kinases involved in cancer cell proliferation. Its halogenated structure allows for selective cross-coupling reactions, enabling the development of novel drug candidates. Also employed in the study of structure-activity relationships (SAR) within imidazopyridazine-based compounds to optimize biological activity and metabolic stability.

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly for targeting tyrosine kinases involved in cancer cell proliferation. Its halogenated structure allows for selective cross-coupling reactions, enabling the development of novel drug candidates. Also employed in the study of structure-activity relationships (SAR) within imidazopyridazine-based compounds to optimize biological activity and metabolic stability.

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