2-Hydroxynicotinaldehyde

97%

Reagent Code: #195210
label
Alias 2-hydroxy nicotinaldehyde; 2-hydroxy-3-aldehyde pyridine; 2-oxo-1,2-dihydropyridine-3-formaldehyde; 2-hydroxy-3-formylpyridine; 2-oxo-1,2-dihydro-3-pyridine
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CAS Number 36404-89-4

science Other reagents with same CAS 36404-89-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 123.11 g/mol
Formula C₆H₅NO₂
thermostat Physical Properties
Melting Point 220-222℃
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of nitrogen-containing heterocyclic compounds. Its aldehyde and hydroxyl functional groups allow for versatile reactivity, enabling condensation and cyclization reactions. Commonly employed in the preparation of fluorescent probes and sensors due to its ability to form conjugated systems that exhibit detectable optical properties. Also finds use in coordination chemistry as a ligand for metal ions, supporting the formation of complexes with potential catalytic or biological activity.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿3,890.00
inventory 10g
10-20 days ฿6,950.00
inventory 25g
10-20 days ฿17,220.00

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2-Hydroxynicotinaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of nitrogen-containing heterocyclic compounds. Its aldehyde and hydroxyl functional groups allow for versatile reactivity, enabling condensation and cyclization reactions. Commonly employed in the preparation of fluorescent probes and sensors due to its ability to form conjugated systems that exhibit detectable optical properties. Also finds use in coordination chemistry as a ligand for metal

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of nitrogen-containing heterocyclic compounds. Its aldehyde and hydroxyl functional groups allow for versatile reactivity, enabling condensation and cyclization reactions. Commonly employed in the preparation of fluorescent probes and sensors due to its ability to form conjugated systems that exhibit detectable optical properties. Also finds use in coordination chemistry as a ligand for metal ions, supporting the formation of complexes with potential catalytic or biological activity.

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