Ethyl 2-iodooxazole-4-carboxylate

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Reagent Code: #182650
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CAS Number 1107663-03-5

science Other reagents with same CAS 1107663-03-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 267.02 g/mol
Formula C₆H₆INO₃
thermostat Physical Properties
Melting Point 113-116°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and heterocyclic compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing oxazole-based drug candidates. Commonly employed in cross-coupling reactions to introduce the oxazole ring into larger molecular frameworks, especially in antifungal, anti-inflammatory, and anticancer agents. Also utilized in agrochemical research for designing novel pesticides and herbicides due to the oxazole core’s metabolic stability and favorable electronic properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,260.00
inventory 250mg
10-20 days ฿2,220.00
inventory 1g
10-20 days ฿9,250.00
inventory 5g
10-20 days ฿19,158.00
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Ethyl 2-iodooxazole-4-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and heterocyclic compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing oxazole-based drug candidates. Commonly employed in cross-coupling reactions to introduce the oxazole ring into larger molecular frameworks, especially in antifungal, anti-inflammatory, and anticancer agents. Also utilized in agrochemical research f

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and heterocyclic compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing oxazole-based drug candidates. Commonly employed in cross-coupling reactions to introduce the oxazole ring into larger molecular frameworks, especially in antifungal, anti-inflammatory, and anticancer agents. Also utilized in agrochemical research for designing novel pesticides and herbicides due to the oxazole core’s metabolic stability and favorable electronic properties.

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