3-Hydroxypyridine-2-carboxaldehyde

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Reagent Code: #194812
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CAS Number 1849-55-4

science Other reagents with same CAS 1849-55-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 123.11 g/mol
Formula C₆H₅NO₂
badge Registry Numbers
MDL Number MFCD06245505
thermostat Physical Properties
Melting Point 80-82°C
Boiling Point 96-100°C
inventory_2 Storage & Handling
Density 1.327 g/cm3
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of antituberculosis agents like isoniazid derivatives. It also serves as a ligand or building block in coordination chemistry and catalysis. Its aldehyde and hydroxyl functional groups allow for easy modification, making it valuable in the development of heterocyclic compounds for medicinal and agrochemical applications. Additionally, it has been explored in the design of enzyme inhibitors and fluorescent probes due to its ability to chelate metal ions and participate in hydrogen bonding.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,200.00
inventory 1g
10-20 days ฿4,760.00
inventory 5g
10-20 days ฿22,700.00

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3-Hydroxypyridine-2-carboxaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of antituberculosis agents like isoniazid derivatives. It also serves as a ligand or building block in coordination chemistry and catalysis. Its aldehyde and hydroxyl functional groups allow for easy modification, making it valuable in the development of heterocyclic compounds for medicinal and agrochemical applications. Additionally, it has been explored in the design of enzyme inhibitors and fluorescent probe

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of antituberculosis agents like isoniazid derivatives. It also serves as a ligand or building block in coordination chemistry and catalysis. Its aldehyde and hydroxyl functional groups allow for easy modification, making it valuable in the development of heterocyclic compounds for medicinal and agrochemical applications. Additionally, it has been explored in the design of enzyme inhibitors and fluorescent probes due to its ability to chelate metal ions and participate in hydrogen bonding.

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