5-Methyl-2-oxo-1,2-dihydropyridine-3-carbaldehyde

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Reagent Code: #129442
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CAS Number 1227575-72-5

science Other reagents with same CAS 1227575-72-5

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scatter_plot Molecular Information
Weight 137.14 g/mol
Formula C₇H₇NO₂
badge Registry Numbers
MDL Number MFCD23135701
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinamide-based drugs and kinase inhibitors. It serves as a building block in medicinal chemistry for constructing pyridone rings, which are common structural motifs in bioactive molecules. Its aldehyde functionality allows for easy derivatization, enabling the formation of imines, oximes, or other functional groups important in drug design. Also employed in the preparation of nootropic agents and compounds targeting neurological disorders. Additionally, it finds use in agrochemical research for developing novel pesticides and herbicides due to its reactive scaffold.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿21,760.00
inventory 250mg
10-20 days ฿36,280.00

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5-Methyl-2-oxo-1,2-dihydropyridine-3-carbaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinamide-based drugs and kinase inhibitors. It serves as a building block in medicinal chemistry for constructing pyridone rings, which are common structural motifs in bioactive molecules. Its aldehyde functionality allows for easy derivatization, enabling the formation of imines, oximes, or other functional groups important in drug design. Also employed in the preparation of nootropic agents and compou

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinamide-based drugs and kinase inhibitors. It serves as a building block in medicinal chemistry for constructing pyridone rings, which are common structural motifs in bioactive molecules. Its aldehyde functionality allows for easy derivatization, enabling the formation of imines, oximes, or other functional groups important in drug design. Also employed in the preparation of nootropic agents and compounds targeting neurological disorders. Additionally, it finds use in agrochemical research for developing novel pesticides and herbicides due to its reactive scaffold.

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