2-Oxo-2-(3-oxo-3,4-dihydroquinoxalin-1(2H)-yl)ethyl (E)-3-(4-methoxyphenyl)acrylate

98%

Reagent Code: #221160
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CAS Number 1164471-66-2

science Other reagents with same CAS 1164471-66-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 366.37 g/mol
Formula C₂₀H₁₈N₂O₅
thermostat Physical Properties
Boiling Point 675.8±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.306±0.06 g/cm3(Predicted)
Storage -20°C, away from light, dry

description Product Description

Used in pharmaceutical research as a synthetic intermediate for kinase inhibitors, particularly in the development of anticancer agents. Its structure supports activity in cell signaling pathway modulation, making it valuable in the design of targeted therapies. Also investigated for use in photodynamic therapy due to its conjugated system and light-responsive properties. Employed in medicinal chemistry for structure-activity relationship (SAR) studies, especially in optimizing quinoxaline-based bioactive molecules.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿18,690.00
100mg
10-20 days ฿40,690.00
2-Oxo-2-(3-oxo-3,4-dihydroquinoxalin-1(2H)-yl)ethyl (E)-3-(4-methoxyphenyl)acrylate
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Used in pharmaceutical research as a synthetic intermediate for kinase inhibitors, particularly in the development of anticancer agents. Its structure supports activity in cell signaling pathway modulation, making it valuable in the design of targeted therapies. Also investigated for use in photodynamic therapy due to its conjugated system and light-responsive properties. Employed in medicinal chemistry for structure-activity relationship (SAR) studies, especially in optimizing quinoxaline-based bioactive m
Used in pharmaceutical research as a synthetic intermediate for kinase inhibitors, particularly in the development of anticancer agents. Its structure supports activity in cell signaling pathway modulation, making it valuable in the design of targeted therapies. Also investigated for use in photodynamic therapy due to its conjugated system and light-responsive properties. Employed in medicinal chemistry for structure-activity relationship (SAR) studies, especially in optimizing quinoxaline-based bioactive molecules.
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