3-Iodo-4-aminopyridine

95%

Reagent Code: #199213
label
Alias 3-Iodine-4-aminopyridine
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CAS Number 88511-27-7

science Other reagents with same CAS 88511-27-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 220.01 g/mol
Formula C₅H₅IN₂
badge Registry Numbers
MDL Number MFCD02663853
thermostat Physical Properties
Melting Point 99.1-99.4°C
inventory_2 Storage & Handling
Storage Room temperature, light-proof, sealed

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and biologically active compounds. Serves as a building block in the preparation of neuroactive agents due to the pyridine core and amino group, which can interact with biological targets. The iodo substituent allows for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry for developing new drug candidates. Also investigated for use in neuroscience research for modifying ion channel function or as a precursor in synthesizing compounds that affect nerve signal transmission.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿950.00
inventory 25g
10-20 days ฿4,090.00
inventory 1g
10-20 days ฿156.00

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3-Iodo-4-aminopyridine
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Used in organic synthesis as an intermediate for pharmaceuticals and biologically active compounds. Serves as a building block in the preparation of neuroactive agents due to the pyridine core and amino group, which can interact with biological targets. The iodo substituent allows for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry for developing new drug candidates. Also investigated for use in neuroscience research for modifying ion channel function or

Used in organic synthesis as an intermediate for pharmaceuticals and biologically active compounds. Serves as a building block in the preparation of neuroactive agents due to the pyridine core and amino group, which can interact with biological targets. The iodo substituent allows for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry for developing new drug candidates. Also investigated for use in neuroscience research for modifying ion channel function or as a precursor in synthesizing compounds that affect nerve signal transmission.

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