3-Iodopyridin-2(1H)-one

98%

Reagent Code: #200674
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CAS Number 111079-46-0

science Other reagents with same CAS 111079-46-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221.00 g/mol
Formula C₅H₄INO
badge Registry Numbers
MDL Number MFCD13192391
thermostat Physical Properties
Boiling Point 350.1±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 2.12±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic acetylcholine receptor modulators. It serves as a building block in medicinal chemistry for creating compounds with neurological activity, including potential treatments for cognitive disorders, pain, and neurodegenerative diseases. Its structure allows for selective functionalization, making it valuable in creating diverse compound libraries for drug discovery. Also employed in cross-coupling reactions such as Suzuki and Heck reactions to form carbon-carbon bonds in heterocyclic systems.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿720.00
inventory 1g
10-20 days ฿2,810.00
inventory 5g
10-20 days ฿11,620.00
inventory 25g
10-20 days ฿44,080.00

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3-Iodopyridin-2(1H)-one
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic acetylcholine receptor modulators. It serves as a building block in medicinal chemistry for creating compounds with neurological activity, including potential treatments for cognitive disorders, pain, and neurodegenerative diseases. Its structure allows for selective functionalization, making it valuable in creating diverse compound libraries for drug discovery. Also employed in cross-coupling rea

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic acetylcholine receptor modulators. It serves as a building block in medicinal chemistry for creating compounds with neurological activity, including potential treatments for cognitive disorders, pain, and neurodegenerative diseases. Its structure allows for selective functionalization, making it valuable in creating diverse compound libraries for drug discovery. Also employed in cross-coupling reactions such as Suzuki and Heck reactions to form carbon-carbon bonds in heterocyclic systems.

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