(3E,5E)-3,5-Bis[(4-nitrophenyl)methylene]-1-(1-oxo-2-propen-1-yl)-4-piperidinone

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Reagent Code: #181894
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CAS Number 1009817-63-3

science Other reagents with same CAS 1009817-63-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 419.38 g/mol
Formula C₂₂H₁₇N₃O₆
inventory_2 Storage & Handling
Storage 2~8°C, sealed

description Product Description

Used as a fluorescent probe in biochemical assays due to its strong electron-withdrawing nitro groups and conjugated structure, enabling detection of reactive oxygen species in cellular environments. Its extended π-conjugation allows for visible-range absorption and emission, making it suitable for imaging applications without requiring UV light. Also investigated as a photosensitizer in photodynamic therapy research, where it generates singlet oxygen upon light activation. Additionally, serves as an intermediate in synthesizing more complex heterocyclic compounds with potential pharmacological activity.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿4,890.00

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(3E,5E)-3,5-Bis[(4-nitrophenyl)methylene]-1-(1-oxo-2-propen-1-yl)-4-piperidinone
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Used as a fluorescent probe in biochemical assays due to its strong electron-withdrawing nitro groups and conjugated structure, enabling detection of reactive oxygen species in cellular environments. Its extended π-conjugation allows for visible-range absorption and emission, making it suitable for imaging applications without requiring UV light. Also investigated as a photosensitizer in photodynamic therapy research, where it generates singlet oxygen upon light activation. Additionally, serves as an int

Used as a fluorescent probe in biochemical assays due to its strong electron-withdrawing nitro groups and conjugated structure, enabling detection of reactive oxygen species in cellular environments. Its extended π-conjugation allows for visible-range absorption and emission, making it suitable for imaging applications without requiring UV light. Also investigated as a photosensitizer in photodynamic therapy research, where it generates singlet oxygen upon light activation. Additionally, serves as an intermediate in synthesizing more complex heterocyclic compounds with potential pharmacological activity.

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