Pyridine-2,3-dicarboxylic acid

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Reagent Code: #226721
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CAS Number 339155-13-4

science Other reagents with same CAS 339155-13-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 167.12 g/mol
Formula C₇H₅NO₄
badge Registry Numbers
MDL Number MFCD00006295
thermostat Physical Properties
Melting Point 188-190 °C (dec.)(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chelating agent in metal ion coordination, forming stable complexes with transition metals for catalysis and material synthesis. Employed in the preparation of pharmaceutical intermediates and nitrogen-containing heterocyclic compounds. Serves as a building block in organic synthesis, particularly in the development of ligands and functionalized pyridine derivatives. Also applied in analytical chemistry for metal ion detection and separation due to its selective binding properties.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿720.00
inventory 100g
10-20 days ฿1,980.00
inventory 500g
10-20 days ฿8,840.00

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Pyridine-2,3-dicarboxylic acid
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Used as a chelating agent in metal ion coordination, forming stable complexes with transition metals for catalysis and material synthesis. Employed in the preparation of pharmaceutical intermediates and nitrogen-containing heterocyclic compounds. Serves as a building block in organic synthesis, particularly in the development of ligands and functionalized pyridine derivatives. Also applied in analytical chemistry for metal ion detection and separation due to its selective binding properties.

Used as a chelating agent in metal ion coordination, forming stable complexes with transition metals for catalysis and material synthesis. Employed in the preparation of pharmaceutical intermediates and nitrogen-containing heterocyclic compounds. Serves as a building block in organic synthesis, particularly in the development of ligands and functionalized pyridine derivatives. Also applied in analytical chemistry for metal ion detection and separation due to its selective binding properties.

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