Ethyl 5-iodonicotinate

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Reagent Code: #130492
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CAS Number 63473-00-7

science Other reagents with same CAS 63473-00-7

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scatter_plot Molecular Information
Weight 277.06 g/mol
Formula C₈H₈INO₂
badge Registry Numbers
MDL Number MFCD12923236
inventory_2 Storage & Handling
Storage 2-8°C, away from light, dry

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals, particularly in the preparation of nicotinic acid derivatives. Its iodine functionality allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex heterocyclic systems. Commonly employed in medicinal chemistry for modifying pyridine-based scaffolds to enhance biological activity or binding properties. Also utilized in the development of kinase inhibitors and other bioactive molecules due to the electron-withdrawing ester group and the reactive iodine handle.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿14,850.00
inventory 100mg
10-20 days ฿8,750.00

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Ethyl 5-iodonicotinate
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Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals, particularly in the preparation of nicotinic acid derivatives. Its iodine functionality allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex heterocyclic systems. Commonly employed in medicinal chemistry for modifying pyridine-based scaffolds to enhance biological activity or binding properties. Also utilized in the development of kinase inhibitors and other bioactive

Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals, particularly in the preparation of nicotinic acid derivatives. Its iodine functionality allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex heterocyclic systems. Commonly employed in medicinal chemistry for modifying pyridine-based scaffolds to enhance biological activity or binding properties. Also utilized in the development of kinase inhibitors and other bioactive molecules due to the electron-withdrawing ester group and the reactive iodine handle.

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