6-Fluoro-4-methylnicotinaldehyde

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Reagent Code: #131974
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CAS Number 1266253-68-2

science Other reagents with same CAS 1266253-68-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 139.13 g/mol
Formula C₇H₆FNO
badge Registry Numbers
MDL Number MFCD18447598
thermostat Physical Properties
Boiling Point 255.4±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.211±0.06 g/cm3(Predicted)
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 nicotinic receptor modulators and fluorinated drug candidates. Its aldehyde functionality allows for versatile chemical transformations, enabling the formation of imines, oximes, and other derivatives important in medicinal chemistry. Commonly employed in the preparation of kinase inhibitors and central nervous system agents due to the enhanced metabolic stability provided by the fluorine substituent. Also utilized in agrochemical research for designing novel bioactive molecules with improved selectivity and potency.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,540.00
inventory 1g
10-20 days ฿4,470.00
inventory 5g
10-20 days ฿15,400.00

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6-Fluoro-4-methylnicotinaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators and fluorinated drug candidates. Its aldehyde functionality allows for versatile chemical transformations, enabling the formation of imines, oximes, and other derivatives important in medicinal chemistry. Commonly employed in the preparation of kinase inhibitors and central nervous system agents due to the enhanced metabolic stability provided by the fluorine substituent. Also

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators and fluorinated drug candidates. Its aldehyde functionality allows for versatile chemical transformations, enabling the formation of imines, oximes, and other derivatives important in medicinal chemistry. Commonly employed in the preparation of kinase inhibitors and central nervous system agents due to the enhanced metabolic stability provided by the fluorine substituent. Also utilized in agrochemical research for designing novel bioactive molecules with improved selectivity and potency.

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