Ethyl 1-(4-methoxyphenyl)-7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine-3-carboxylate

≥95%

Reagent Code: #183488
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CAS Number 503614-56-0

science Other reagents with same CAS 503614-56-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 315.32 g/mol
Formula C₁₆H₁₇N₃O₄
badge Registry Numbers
MDL Number MFCD21340322
thermostat Physical Properties
Boiling Point 588.554°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry seal

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly in the development of kinase inhibitors. Its structure supports the design of molecules with potential anti-inflammatory, anticancer, and central nervous system-modulating activities. Commonly employed in medicinal chemistry for scaffold modification and structure-activity relationship (SAR) studies due to its fused heterocyclic core and functional handles for derivatization.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿15,390.00
inventory 250mg
10-20 days ฿30,780.00

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Ethyl 1-(4-methoxyphenyl)-7-oxo-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine-3-carboxylate
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Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly in the development of kinase inhibitors. Its structure supports the design of molecules with potential anti-inflammatory, anticancer, and central nervous system-modulating activities. Commonly employed in medicinal chemistry for scaffold modification and structure-activity relationship (SAR) studies due to its fused heterocyclic core and functional handles for derivatization.

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly in the development of kinase inhibitors. Its structure supports the design of molecules with potential anti-inflammatory, anticancer, and central nervous system-modulating activities. Commonly employed in medicinal chemistry for scaffold modification and structure-activity relationship (SAR) studies due to its fused heterocyclic core and functional handles for derivatization.

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