5-Bromo-3-iodopyridin-2(1H)-one

95%

Reagent Code: #145375
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CAS Number 381233-75-6

science Other reagents with same CAS 381233-75-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 299.89 g/mol
Formula C₅H₃BrINO
thermostat Physical Properties
Melting Point 226-227°C
Boiling Point 316.3°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its halogen substituents allow for selective cross-coupling reactions, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in Suzuki and Heck reactions to introduce aryl or vinyl groups during drug discovery processes. Also utilized in the preparation of pyridone-based derivatives with potential antiviral or anticancer activity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿165.00
inventory 5g
10-20 days ฿396.00
inventory 25g
10-20 days ฿1,963.50
inventory 100g
10-20 days ฿7,843.00
inventory 1g
10-20 days ฿137.50

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5-Bromo-3-iodopyridin-2(1H)-one
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its halogen substituents allow for selective cross-coupling reactions, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in Suzuki and Heck reactions to introduce aryl or vinyl groups during drug discovery processes. Also utilized in the preparation of pyridone-based derivatives with potential

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its halogen substituents allow for selective cross-coupling reactions, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in Suzuki and Heck reactions to introduce aryl or vinyl groups during drug discovery processes. Also utilized in the preparation of pyridone-based derivatives with potential antiviral or anticancer activity.

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