Methyl 5-fluoro-2-methoxynicotinate

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Reagent Code: #202891
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CAS Number 122433-52-7

science Other reagents with same CAS 122433-52-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 185.15 g/mol
Formula C₈H₈FNO₃
badge Registry Numbers
MDL Number MFCD14698160
thermostat Physical Properties
Boiling Point 237.9±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.244±0.06 g/cm3(Predicted)
Storage Room temperature, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure supports the construction of nitrogen-containing heterocycles, which are common motifs in drug discovery. The fluorine and methoxy groups enhance binding selectivity and metabolic stability, making it valuable in optimizing lead compounds for improved potency and pharmacokinetics. Commonly employed in medicinal chemistry research for generating analogs in structure-activity relationship (SAR) studies.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿26,400.00
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Methyl 5-fluoro-2-methoxynicotinate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure supports the construction of nitrogen-containing heterocycles, which are common motifs in drug discovery. The fluorine and methoxy groups enhance binding selectivity and metabolic stability, making it valuable in optimizing lead compounds for improved potency and pharmacokinetics. Commonly employed in medicinal chemistry research for g

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure supports the construction of nitrogen-containing heterocycles, which are common motifs in drug discovery. The fluorine and methoxy groups enhance binding selectivity and metabolic stability, making it valuable in optimizing lead compounds for improved potency and pharmacokinetics. Commonly employed in medicinal chemistry research for generating analogs in structure-activity relationship (SAR) studies.

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