Methyl 3-fluoroisonicotinate

96%

Reagent Code: #210384
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CAS Number 876919-08-3

science Other reagents with same CAS 876919-08-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 155.13 g/mol
Formula C₇H₆FNO₂
badge Registry Numbers
MDL Number MFCD11045048
thermostat Physical Properties
Boiling Point 206.8 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its fluorinated pyridine core enhances binding affinity and metabolic stability in drug candidates. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the electron-withdrawing effect of the fluorine atom, which influences reactivity and pharmacokinetic properties. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and selectivity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,400.00
inventory 5g
10-20 days ฿6,800.00
inventory 10g
10-20 days ฿10,200.00
inventory 25g
10-20 days ฿22,400.00
inventory 100g
10-20 days ฿76,800.00

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Methyl 3-fluoroisonicotinate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its fluorinated pyridine core enhances binding affinity and metabolic stability in drug candidates. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the electron-withdrawing effect of the fluorine atom, which influences reactivity and pharmacokinetic properties. Also utilized in agrochemical research for design

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its fluorinated pyridine core enhances binding affinity and metabolic stability in drug candidates. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the electron-withdrawing effect of the fluorine atom, which influences reactivity and pharmacokinetic properties. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and selectivity.

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