5-Hydroxy-4-oxo-1,4-dihydropyridine-2-carboxylic acid

≥95%

Reagent Code: #195588
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CAS Number 43077-77-6

science Other reagents with same CAS 43077-77-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 155.11 g/mol
Formula C₆H₅NO₄
badge Registry Numbers
MDL Number MFCD01646063
thermostat Physical Properties
Boiling Point 374.6°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.708g/cm3
Storage 2-8°C, stored in inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of nicotinamide analogs and enzyme inhibitors. It plays a role in research related to NAD+ metabolism and redox biology due to its structural similarity to pyridine nucleotides. Also investigated for potential applications in designing antimicrobial and antiviral agents. Its keto and hydroxyl functional groups allow for derivatization in medicinal chemistry campaigns targeting metabolic enzymes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,970.00
inventory 250mg
10-20 days ฿22,420.00

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5-Hydroxy-4-oxo-1,4-dihydropyridine-2-carboxylic acid
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of nicotinamide analogs and enzyme inhibitors. It plays a role in research related to NAD+ metabolism and redox biology due to its structural similarity to pyridine nucleotides. Also investigated for potential applications in designing antimicrobial and antiviral agents. Its keto and hydroxyl functional groups allow for derivatization in medicinal chemistry campaigns targeting metabolic enzymes.

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of nicotinamide analogs and enzyme inhibitors. It plays a role in research related to NAD+ metabolism and redox biology due to its structural similarity to pyridine nucleotides. Also investigated for potential applications in designing antimicrobial and antiviral agents. Its keto and hydroxyl functional groups allow for derivatization in medicinal chemistry campaigns targeting metabolic enzymes.

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