Ethyl 3-(4-fluorophenyl)-5-methylisoxazole-4-carboxylate

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Reagent Code: #182517
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CAS Number 954230-39-8

science Other reagents with same CAS 954230-39-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 249.24 g/mol
Formula C₁₃H₁₂FNO₃
badge Registry Numbers
MDL Number MFCD09756447
thermostat Physical Properties
Boiling Point 370.5°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and central nervous system (CNS) active compounds. Its structure supports the construction of bioactive molecules due to the presence of the isoxazole ring and fluorinated aryl group, which enhance metabolic stability and binding affinity. Commonly employed in medicinal chemistry for optimizing lead compounds in drug discovery programs targeting neurological disorders and pain management. Also utilized in the preparation of selective enzyme inhibitors and receptor modulators.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,920.00
inventory 250mg
10-20 days ฿4,790.00
inventory 5g
10-20 days ฿28,880.00
inventory 1g
10-20 days ฿9,600.00

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Ethyl 3-(4-fluorophenyl)-5-methylisoxazole-4-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and central nervous system (CNS) active compounds. Its structure supports the construction of bioactive molecules due to the presence of the isoxazole ring and fluorinated aryl group, which enhance metabolic stability and binding affinity. Commonly employed in medicinal chemistry for optimizing lead compounds in drug discovery programs targeting neurological disorders and pain manage

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and central nervous system (CNS) active compounds. Its structure supports the construction of bioactive molecules due to the presence of the isoxazole ring and fluorinated aryl group, which enhance metabolic stability and binding affinity. Commonly employed in medicinal chemistry for optimizing lead compounds in drug discovery programs targeting neurological disorders and pain management. Also utilized in the preparation of selective enzyme inhibitors and receptor modulators.

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