Methyl 5-hydroxy-6-iodonicotinate

≥95%

Reagent Code: #61410
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CAS Number 1189816-87-2

science Other reagents with same CAS 1189816-87-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 279.03 g/mol
Formula C₇H₆INO₃
badge Registry Numbers
MDL Number MFCD27942050
inventory_2 Storage & Handling
Storage 2-8°C, dry, airtight

description Product Description

Methyl 5-hydroxy-6-iodonicotinate is primarily utilized in organic synthesis as a versatile intermediate. It plays a significant role in the development of pharmaceuticals, particularly in the synthesis of complex molecules with potential therapeutic properties. The compound is often employed in cross-coupling reactions, where its iodine moiety facilitates the formation of carbon-carbon or carbon-heteroatom bonds, essential for constructing biologically active compounds. Additionally, its hydroxyl and ester functional groups make it a valuable building block for modifying and optimizing drug candidates. Researchers also explore its use in material science for creating specialized organic materials with unique electronic or optical properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,680.00
inventory 1g
10-20 days ฿12,060.00
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Methyl 5-hydroxy-6-iodonicotinate
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Methyl 5-hydroxy-6-iodonicotinate is primarily utilized in organic synthesis as a versatile intermediate. It plays a significant role in the development of pharmaceuticals, particularly in the synthesis of complex molecules with potential therapeutic properties. The compound is often employed in cross-coupling reactions, where its iodine moiety facilitates the formation of carbon-carbon or carbon-heteroatom bonds, essential for constructing biologically active compounds. Additionally, its hydroxyl and es

Methyl 5-hydroxy-6-iodonicotinate is primarily utilized in organic synthesis as a versatile intermediate. It plays a significant role in the development of pharmaceuticals, particularly in the synthesis of complex molecules with potential therapeutic properties. The compound is often employed in cross-coupling reactions, where its iodine moiety facilitates the formation of carbon-carbon or carbon-heteroatom bonds, essential for constructing biologically active compounds. Additionally, its hydroxyl and ester functional groups make it a valuable building block for modifying and optimizing drug candidates. Researchers also explore its use in material science for creating specialized organic materials with unique electronic or optical properties.

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