7-[2-[2,5-Dimethyl-1-(thiophen-2-ylmethyl)pyrrol-3-yl]-2-oxoethoxy]chromen-2-one

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Reagent Code: #245747
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CAS Number 869354-02-9

science Other reagents with same CAS 869354-02-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 393.5 g/mol
Formula C₂₂H₁₉NO₄S
thermostat Physical Properties
Boiling Point 628.8±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.29±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a fluorescent probe in biochemical and analytical applications due to its strong fluorescence properties. It binds selectively to specific proteins or enzymes, making it useful in studying enzyme activity and molecular interactions. Commonly employed in assays for monitoring esterase activity, where enzymatic cleavage releases the fluorescent chromone derivative, allowing real-time detection. Also applied in cellular imaging for tracking biological processes in live cells. Its thiophene and pyrrole moieties enhance stability and binding specificity, improving sensitivity in detection systems.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿16,490.00
inventory 5mg
10-20 days ฿9,890.00
inventory 25mg
10-20 days ฿32,990.00

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7-[2-[2,5-Dimethyl-1-(thiophen-2-ylmethyl)pyrrol-3-yl]-2-oxoethoxy]chromen-2-one
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Used as a fluorescent probe in biochemical and analytical applications due to its strong fluorescence properties. It binds selectively to specific proteins or enzymes, making it useful in studying enzyme activity and molecular interactions. Commonly employed in assays for monitoring esterase activity, where enzymatic cleavage releases the fluorescent chromone derivative, allowing real-time detection. Also applied in cellular imaging for tracking biological processes in live cells. Its thiophene and pyrro

Used as a fluorescent probe in biochemical and analytical applications due to its strong fluorescence properties. It binds selectively to specific proteins or enzymes, making it useful in studying enzyme activity and molecular interactions. Commonly employed in assays for monitoring esterase activity, where enzymatic cleavage releases the fluorescent chromone derivative, allowing real-time detection. Also applied in cellular imaging for tracking biological processes in live cells. Its thiophene and pyrrole moieties enhance stability and binding specificity, improving sensitivity in detection systems.

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