N-Benzyl-2-oxo-3-(phenylsulfonyl)-2H-chromene-6-carboxamide

98%

Reagent Code: #214752
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CAS Number 904449-84-9

science Other reagents with same CAS 904449-84-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 419.45 g/mol
Formula C₂₃H₁₇NO₅S
badge Registry Numbers
MDL Number MFCD14772424
thermostat Physical Properties
Boiling Point 702.3±60.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.382±0.06 g/cm3(Predicted)
Storage -20°C, Sealed, Dry

description Product Description

Used as a key intermediate in the synthesis of anticoagulant and anti-inflammatory agents. Exhibits strong inhibitory activity against certain serine proteases involved in blood coagulation pathways, making it valuable in developing novel antithrombotic drugs. Also shows potential in medicinal chemistry for designing enzyme inhibitors due to its ability to interact with sulfonamide and lactone moieties in biological targets. Commonly employed in structure-activity relationship (SAR) studies for optimizing pharmacokinetic properties in drug discovery programs.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿19,860.00
inventory 50mg
10-20 days ฿59,540.00

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N-Benzyl-2-oxo-3-(phenylsulfonyl)-2H-chromene-6-carboxamide
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Used as a key intermediate in the synthesis of anticoagulant and anti-inflammatory agents. Exhibits strong inhibitory activity against certain serine proteases involved in blood coagulation pathways, making it valuable in developing novel antithrombotic drugs. Also shows potential in medicinal chemistry for designing enzyme inhibitors due to its ability to interact with sulfonamide and lactone moieties in biological targets. Commonly employed in structure-activity relationship (SAR) studies for optimizing p
Used as a key intermediate in the synthesis of anticoagulant and anti-inflammatory agents. Exhibits strong inhibitory activity against certain serine proteases involved in blood coagulation pathways, making it valuable in developing novel antithrombotic drugs. Also shows potential in medicinal chemistry for designing enzyme inhibitors due to its ability to interact with sulfonamide and lactone moieties in biological targets. Commonly employed in structure-activity relationship (SAR) studies for optimizing pharmacokinetic properties in drug discovery programs.
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