Ethyl 5-Methylisoxazole-3-Carboxylate

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Reagent Code: #182979
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CAS Number 3209-72-1

science Other reagents with same CAS 3209-72-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 155.15 g/mol
Formula C₇H₉NO₃
badge Registry Numbers
MDL Number MFCD00085080
thermostat Physical Properties
Melting Point 25 °C
Boiling Point 77-79°C 0,5mm
inventory_2 Storage & Handling
Density 1.139g/cm3
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of certain central nervous system agents and nootropic drugs. It serves as a building block in heterocyclic chemistry due to the reactivity of the isoxazole ring, enabling functionalization for drug development. Commonly employed in research settings to develop compounds with potential cognitive-enhancing or neuroprotective properties. Its ester group allows for easy modification, making it valuable in medicinal chemistry for structure-activity relationship studies.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿590.00
inventory 5g
10-20 days ฿1,950.00
inventory 25g
10-20 days ฿8,870.00
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Ethyl 5-Methylisoxazole-3-Carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of certain central nervous system agents and nootropic drugs. It serves as a building block in heterocyclic chemistry due to the reactivity of the isoxazole ring, enabling functionalization for drug development. Commonly employed in research settings to develop compounds with potential cognitive-enhancing or neuroprotective properties. Its ester group allows for easy modification, making it valuable in medicina

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of certain central nervous system agents and nootropic drugs. It serves as a building block in heterocyclic chemistry due to the reactivity of the isoxazole ring, enabling functionalization for drug development. Commonly employed in research settings to develop compounds with potential cognitive-enhancing or neuroprotective properties. Its ester group allows for easy modification, making it valuable in medicinal chemistry for structure-activity relationship studies.

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