Ethyl 5-chloro-4-hydroxy-1-methyl-2-oxo-1,2-dihydroquinoline-3-carboxylate

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Reagent Code: #131452
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CAS Number 248282-10-2

science Other reagents with same CAS 248282-10-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 281.69 g/mol
Formula C₁₃H₁₂ClNO₄
thermostat Physical Properties
Boiling Point 419.0±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.436±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs) and related pharmaceuticals. Its structure supports the development of compounds with analgesic and antipyretic properties. Commonly employed in medicinal chemistry for constructing quinoline-based drug candidates targeting enzyme inhibition, particularly in cyclooxygenase (COX) inhibitor research. Also utilized in the preparation of derivatives for biological activity screening in anti-inflammatory and anticancer studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿21,750.00
inventory 250mg
10-20 days ฿36,950.00

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Ethyl 5-chloro-4-hydroxy-1-methyl-2-oxo-1,2-dihydroquinoline-3-carboxylate
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Used as a key intermediate in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs) and related pharmaceuticals. Its structure supports the development of compounds with analgesic and antipyretic properties. Commonly employed in medicinal chemistry for constructing quinoline-based drug candidates targeting enzyme inhibition, particularly in cyclooxygenase (COX) inhibitor research. Also utilized in the preparation of derivatives for biological activity screening in anti-inflammatory and anticanc

Used as a key intermediate in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs) and related pharmaceuticals. Its structure supports the development of compounds with analgesic and antipyretic properties. Commonly employed in medicinal chemistry for constructing quinoline-based drug candidates targeting enzyme inhibition, particularly in cyclooxygenase (COX) inhibitor research. Also utilized in the preparation of derivatives for biological activity screening in anti-inflammatory and anticancer studies.

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