Ethyl 1H-pyrazolo[4,3-b]pyridine-3-carboxylate

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Reagent Code: #183529
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CAS Number 1234616-14-8

science Other reagents with same CAS 1234616-14-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 191.19 g/mol
Formula C₉H₉N₃O₂
badge Registry Numbers
MDL Number MFCD16658534
thermostat Physical Properties
Boiling Point 369°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly kinase inhibitors. It serves as a building block for drug candidates targeting inflammatory diseases, cancer, and central nervous system disorders. Its structure supports the development of molecules with high selectivity and potency due to favorable interactions with enzyme binding sites. Also employed in medicinal chemistry for scaffold modification and structure-activity relationship (SAR) studies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,850.00
inventory 1g
10-20 days ฿7,280.00
inventory 100mg
10-20 days ฿1,540.00

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Ethyl 1H-pyrazolo[4,3-b]pyridine-3-carboxylate
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Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly kinase inhibitors. It serves as a building block for drug candidates targeting inflammatory diseases, cancer, and central nervous system disorders. Its structure supports the development of molecules with high selectivity and potency due to favorable interactions with enzyme binding sites. Also employed in medicinal chemistry for scaffold modification and structure-activity relationship (

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly kinase inhibitors. It serves as a building block for drug candidates targeting inflammatory diseases, cancer, and central nervous system disorders. Its structure supports the development of molecules with high selectivity and potency due to favorable interactions with enzyme binding sites. Also employed in medicinal chemistry for scaffold modification and structure-activity relationship (SAR) studies.

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