2-(Pyridin-4-yl)acetic acid

98%

Reagent Code: #226754
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CAS Number 28356-58-3

science Other reagents with same CAS 28356-58-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 137.14 g/mol
Formula C₇H₇NO₂
badge Registry Numbers
MDL Number MFCD03701446
thermostat Physical Properties
Melting Point 139-141 °C (lit.)
Boiling Point 303.8 °C at 760 mmHg (lit.)
inventory_2 Storage & Handling
Storage 2-8°C, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of nicotinic receptor ligands and drugs targeting neurological disorders. It serves as a building block in medicinal chemistry for developing compounds with potential cognitive-enhancing or neuroprotective effects. Also employed in the preparation of pyridine-based agrochemicals and specialty polymers due to its ability to form stable coordination complexes and participate in coupling reactions. Its carboxylic acid group allows easy derivatization into esters, amides, and other functional groups for tailored applications in research and development.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,450.00
inventory 5g
10-20 days ฿6,350.00
inventory 25g
10-20 days ฿29,370.00

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2-(Pyridin-4-yl)acetic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of nicotinic receptor ligands and drugs targeting neurological disorders. It serves as a building block in medicinal chemistry for developing compounds with potential cognitive-enhancing or neuroprotective effects. Also employed in the preparation of pyridine-based agrochemicals and specialty polymers due to its ability to form stable coordination complexes and participate in coupling reactions. Its carboxylic

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of nicotinic receptor ligands and drugs targeting neurological disorders. It serves as a building block in medicinal chemistry for developing compounds with potential cognitive-enhancing or neuroprotective effects. Also employed in the preparation of pyridine-based agrochemicals and specialty polymers due to its ability to form stable coordination complexes and participate in coupling reactions. Its carboxylic acid group allows easy derivatization into esters, amides, and other functional groups for tailored applications in research and development.

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