2-(4-Oxopyridin-1(4H)-yl)acetic acid

≥95%

Reagent Code: #220974
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CAS Number 45965-36-4

science Other reagents with same CAS 45965-36-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 153.1387 g/mol
Formula C₇H₇NO₃
badge Registry Numbers
MDL Number MFCD01646172
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinamide-based compounds with potential metabolic and neurological activity. It serves as a building block for pyridinone derivatives, which are explored for their enzyme inhibitory properties. Also employed in research related to NAD+ metabolism modulators due to its structural similarity to nicotinamide. Its acetic acid side chain allows for easy functionalization, making it useful in medicinal chemistry for creating analogs and probing structure-activity relationships.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿13,180.00
inventory 5g
10-20 days ฿46,100.00

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2-(4-Oxopyridin-1(4H)-yl)acetic acid
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinamide-based compounds with potential metabolic and neurological activity. It serves as a building block for pyridinone derivatives, which are explored for their enzyme inhibitory properties. Also employed in research related to NAD+ metabolism modulators due to its structural similarity to nicotinamide. Its acetic acid side chain allows for easy functionalization, making it useful in medicinal chemistry

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinamide-based compounds with potential metabolic and neurological activity. It serves as a building block for pyridinone derivatives, which are explored for their enzyme inhibitory properties. Also employed in research related to NAD+ metabolism modulators due to its structural similarity to nicotinamide. Its acetic acid side chain allows for easy functionalization, making it useful in medicinal chemistry for creating analogs and probing structure-activity relationships.

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