(E)-3-(4-(Furan-2-yl)-2-oxobut-3-en-1-yl)-3-hydroxyindolin-2-one

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Reagent Code: #181077
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CAS Number 1609385-99-0

science Other reagents with same CAS 1609385-99-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 283.28 g/mol
Formula C₁₆H₁₃NO₄
thermostat Physical Properties
Boiling Point 555.4±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.353±0.06 g/cm3(Predicted)
Storage -20°C, Sealed, Dry

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Shows potential in the development of anti-inflammatory and anticancer agents due to its structural similarity to active kinase inhibitors. Also employed in research focused on heterocyclic compounds for drug discovery, particularly in designing molecules with enhanced binding affinity to specific enzyme targets. Its conjugated system makes it suitable for studies in photophysical properties and sensor development.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿58,230.00
inventory 250mg
10-20 days ฿98,990.00

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(E)-3-(4-(Furan-2-yl)-2-oxobut-3-en-1-yl)-3-hydroxyindolin-2-one
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Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Shows potential in the development of anti-inflammatory and anticancer agents due to its structural similarity to active kinase inhibitors. Also employed in research focused on heterocyclic compounds for drug discovery, particularly in designing molecules with enhanced binding affinity to specific enzyme targets. Its conjugated system makes it suitable for studies in photophysical properties and sensor development.<

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Shows potential in the development of anti-inflammatory and anticancer agents due to its structural similarity to active kinase inhibitors. Also employed in research focused on heterocyclic compounds for drug discovery, particularly in designing molecules with enhanced binding affinity to specific enzyme targets. Its conjugated system makes it suitable for studies in photophysical properties and sensor development.

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