6-Chloro-4-iodonicotinic acid

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Reagent Code: #164205
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CAS Number 1211578-80-1

science Other reagents with same CAS 1211578-80-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 283.45 g/mol
Formula C₆H₃ClINO₂
badge Registry Numbers
MDL Number MFCD18259173
thermostat Physical Properties
Boiling Point 380.7±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 2.193±0.06 g/cm3(Predicted)
Storage 2-8°C, avoiding light

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor ligands and agrochemicals. Its halogenated structure makes it valuable for cross-coupling reactions in organic synthesis, enabling the construction of complex heterocyclic systems. Commonly employed in medicinal chemistry for modifying bioavailability and binding affinity of drug candidates. Also utilized in the preparation of functionalized pyridine derivatives for use in crop protection agents and kinase inhibitors.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,340.00
inventory 1g
10-20 days ฿15,290.00
inventory 5g
10-20 days ฿46,800.00
inventory 100mg
10-20 days ฿2,560.00

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6-Chloro-4-iodonicotinic acid
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor ligands and agrochemicals. Its halogenated structure makes it valuable for cross-coupling reactions in organic synthesis, enabling the construction of complex heterocyclic systems. Commonly employed in medicinal chemistry for modifying bioavailability and binding affinity of drug candidates. Also utilized in the preparation of functionalized pyridine derivatives for use in crop protection ag

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor ligands and agrochemicals. Its halogenated structure makes it valuable for cross-coupling reactions in organic synthesis, enabling the construction of complex heterocyclic systems. Commonly employed in medicinal chemistry for modifying bioavailability and binding affinity of drug candidates. Also utilized in the preparation of functionalized pyridine derivatives for use in crop protection agents and kinase inhibitors.

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