5-(Benzyloxy)-2-(hydroxymethyl)pyridin-4(1H)-one

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Reagent Code: #119821
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CAS Number 59281-14-0

science Other reagents with same CAS 59281-14-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 231.25 g/mol
Formula C₁₃H₁₃NO₃
badge Registry Numbers
MDL Number MFCD00100501
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. Its structure is particularly valuable in the development of drugs targeting neurological and inflammatory disorders. Researchers leverage its pyridine core and functional groups to design molecules that can interact with specific biological targets, such as enzymes or receptors, to modulate their activity. Additionally, it plays a role in the creation of prodrugs, where its hydroxyl and benzyloxy groups can be modified to improve drug delivery and bioavailability. Its application extends to organic synthesis, where it serves as a building block for constructing complex molecules with potential therapeutic properties.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,925.00
inventory 250mg
10-20 days ฿1,467.00

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5-(Benzyloxy)-2-(hydroxymethyl)pyridin-4(1H)-one
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. Its structure is particularly valuable in the development of drugs targeting neurological and inflammatory disorders. Researchers leverage its pyridine core and functional groups to design molecules that can interact with specific biological targets, such as enzymes or receptors, to modulate their activity. Additionally, it plays a role in the creation of prodru

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. Its structure is particularly valuable in the development of drugs targeting neurological and inflammatory disorders. Researchers leverage its pyridine core and functional groups to design molecules that can interact with specific biological targets, such as enzymes or receptors, to modulate their activity. Additionally, it plays a role in the creation of prodrugs, where its hydroxyl and benzyloxy groups can be modified to improve drug delivery and bioavailability. Its application extends to organic synthesis, where it serves as a building block for constructing complex molecules with potential therapeutic properties.

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