(7,8-Dimethyl-2-oxo-2H-chromen-4-yl)methyl (2-fluorobenzoyl)glycinate

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Reagent Code: #157472
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CAS Number 868269-33-4

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 383.37 g/mol
Formula C₂₁H₁₈FNO₅
thermostat Physical Properties
Boiling Point 603.2±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.303±0.06 g/cm3(Predicted)
Storage -20°C, Sealed, Dry

description Product Description

Used as a fluorescent probe in biochemical assays due to its coumarin core, enabling detection of enzyme activity and molecular interactions in cellular environments. Its fluorobenzoyl group enhances binding selectivity toward specific esterases and proteases, making it valuable in drug metabolism studies. Also employed in imaging applications for real-time monitoring of hydrolysis reactions in live cells. Shows potential in targeted drug delivery systems where controlled release is triggered by enzymatic cleavage of the glycinate ester bond.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿10,330.00
inventory 10mg
10-20 days ฿17,590.00
inventory 25mg
10-20 days ฿32,990.00

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(7,8-Dimethyl-2-oxo-2H-chromen-4-yl)methyl (2-fluorobenzoyl)glycinate
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Used as a fluorescent probe in biochemical assays due to its coumarin core, enabling detection of enzyme activity and molecular interactions in cellular environments. Its fluorobenzoyl group enhances binding selectivity toward specific esterases and proteases, making it valuable in drug metabolism studies. Also employed in imaging applications for real-time monitoring of hydrolysis reactions in live cells. Shows potential in targeted drug delivery systems where controlled release is triggered by enzymati

Used as a fluorescent probe in biochemical assays due to its coumarin core, enabling detection of enzyme activity and molecular interactions in cellular environments. Its fluorobenzoyl group enhances binding selectivity toward specific esterases and proteases, making it valuable in drug metabolism studies. Also employed in imaging applications for real-time monitoring of hydrolysis reactions in live cells. Shows potential in targeted drug delivery systems where controlled release is triggered by enzymatic cleavage of the glycinate ester bond.

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