2-Iodo-3-hydroxypyridine

98%

Reagent Code: #199281
label
Alias 2-Iodine-3-pyridinol
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CAS Number 40263-57-8

science Other reagents with same CAS 40263-57-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221 g/mol
Formula C₅H₄INO
badge Registry Numbers
EC Number 254-864-0
MDL Number MFCD00023421
thermostat Physical Properties
Melting Point 193-195°C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic acetylcholine receptor modulators. It serves as a building block in the preparation of compounds with potential neurological activity, including treatments for cognitive disorders and neuropathic pain. Also employed in research settings for the construction of heterocyclic compounds due to its reactive iodine and hydroxyl functional groups, enabling cross-coupling reactions and derivatization.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿174.00
inventory 5g
10-20 days ฿520.00
inventory 25g
10-20 days ฿1,380.00
inventory 100g
10-20 days ฿8,210.00

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2-Iodo-3-hydroxypyridine
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic acetylcholine receptor modulators. It serves as a building block in the preparation of compounds with potential neurological activity, including treatments for cognitive disorders and neuropathic pain. Also employed in research settings for the construction of heterocyclic compounds due to its reactive iodine and hydroxyl functional groups, enabling cross-coupling reactions and derivatization.
Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic acetylcholine receptor modulators. It serves as a building block in the preparation of compounds with potential neurological activity, including treatments for cognitive disorders and neuropathic pain. Also employed in research settings for the construction of heterocyclic compounds due to its reactive iodine and hydroxyl functional groups, enabling cross-coupling reactions and derivatization.
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