Ethyl 5-hydroxy-3-methylisoxazole-4-carboxylate

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Reagent Code: #180588
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CAS Number 133827-50-6

science Other reagents with same CAS 133827-50-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 171.15 g/mol
Formula C₇H₉NO₄
badge Registry Numbers
MDL Number MFCD24394828
thermostat Physical Properties
Boiling Point 257.6±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.271±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, 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-active compounds. Its structure supports derivatization for enhancing drug potency and selectivity. Commonly employed in medicinal chemistry for building heterocyclic frameworks found in bioactive molecules. Also utilized in research settings to design novel isoxazole-based therapeutics with improved metabolic stability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,740.00
inventory 1g
10-20 days ฿12,530.00

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Ethyl 5-hydroxy-3-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-active compounds. Its structure supports derivatization for enhancing drug potency and selectivity. Commonly employed in medicinal chemistry for building heterocyclic frameworks found in bioactive molecules. Also utilized in research settings to design novel isoxazole-based therapeutics with improved metabolic stability.

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and central nervous system-active compounds. Its structure supports derivatization for enhancing drug potency and selectivity. Commonly employed in medicinal chemistry for building heterocyclic frameworks found in bioactive molecules. Also utilized in research settings to design novel isoxazole-based therapeutics with improved metabolic stability.

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