4-((5-Chloro-6-oxo-1-phenyl-1,6-dihydropyridazin-4-yl)oxy)-3-methoxybenzaldehyde

98%

Reagent Code: #166252
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CAS Number 839685-25-5

science Other reagents with same CAS 839685-25-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 356.76 g/mol
Formula C₁₈H₁₃ClN₂O₄
badge Registry Numbers
MDL Number MFCD06196524
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification to enhance binding affinity to specific enzyme targets. Commonly employed in medicinal chemistry research to optimize drug candidates targeting inflammatory diseases and tumor growth. Also utilized in the preparation of fluorescent probes due to its aldehyde functional group, enabling conjugation with biomolecules for imaging applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,010.00

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4-((5-Chloro-6-oxo-1-phenyl-1,6-dihydropyridazin-4-yl)oxy)-3-methoxybenzaldehyde
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification to enhance binding affinity to specific enzyme targets. Commonly employed in medicinal chemistry research to optimize drug candidates targeting inflammatory diseases and tumor growth. Also utilized in the preparation of fluorescent probes due to its aldehyde functional group, enabling conjugation with biomolecules

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification to enhance binding affinity to specific enzyme targets. Commonly employed in medicinal chemistry research to optimize drug candidates targeting inflammatory diseases and tumor growth. Also utilized in the preparation of fluorescent probes due to its aldehyde functional group, enabling conjugation with biomolecules for imaging applications.

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