4-((4-Oxochroman-3-ylidene)methyl)benzoic acid

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Reagent Code: #220968
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CAS Number 556034-11-8

science Other reagents with same CAS 556034-11-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 280.27 g/mol
Formula C₁₇H₁₂O₄
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of anticoagulant drugs, particularly in the production of novel vitamin K antagonists. It serves as a building block for coumarin-based derivatives that exhibit strong blood-thinning properties. Its structure allows for easy modification to enhance pharmacokinetic properties such as bioavailability and metabolic stability. Also explored in medicinal chemistry for developing new anti-thrombotic agents with improved safety profiles. Additionally, it finds use in research settings for structure-activity relationship (SAR) studies of coumarin analogs.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿20,170.00
inventory 1g
10-20 days ฿54,450.00
inventory 5g
10-20 days ฿190,580.00

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4-((4-Oxochroman-3-ylidene)methyl)benzoic acid
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Used as a key intermediate in the synthesis of anticoagulant drugs, particularly in the production of novel vitamin K antagonists. It serves as a building block for coumarin-based derivatives that exhibit strong blood-thinning properties. Its structure allows for easy modification to enhance pharmacokinetic properties such as bioavailability and metabolic stability. Also explored in medicinal chemistry for developing new anti-thrombotic agents with improved safety profiles. Additionally, it finds use in

Used as a key intermediate in the synthesis of anticoagulant drugs, particularly in the production of novel vitamin K antagonists. It serves as a building block for coumarin-based derivatives that exhibit strong blood-thinning properties. Its structure allows for easy modification to enhance pharmacokinetic properties such as bioavailability and metabolic stability. Also explored in medicinal chemistry for developing new anti-thrombotic agents with improved safety profiles. Additionally, it finds use in research settings for structure-activity relationship (SAR) studies of coumarin analogs.

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