Methyl 5-bromo-3-fluoropicolinate

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Reagent Code: #210370
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CAS Number 1211538-72-5

science Other reagents with same CAS 1211538-72-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.02 g/mol
Formula C₇H₅BrFNO₂
badge Registry Numbers
MDL Number MFCD14698121
thermostat Physical Properties
Boiling Point 287.1±40.0 °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 agrochemicals, particularly herbicides and insecticides, due to the presence of reactive halogen atoms that enable further functionalization. The ester group facilitates coupling reactions in organic synthesis, making it valuable in the development of active pharmaceutical ingredients (APIs). Its fluorinated and brominated structure enhances binding selectivity in bioactive molecules, often exploited in crop protection research and medicinal chemistry for designing novel compounds with improved metabolic stability and potency.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿900.00
inventory 250mg
10-20 days ฿1,840.00
inventory 1g
10-20 days ฿3,350.00
inventory 5g
10-20 days ฿15,320.00
inventory 10g
10-20 days ฿30,400.00
inventory 25g
10-20 days ฿51,490.00

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Methyl 5-bromo-3-fluoropicolinate
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Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to the presence of reactive halogen atoms that enable further functionalization. The ester group facilitates coupling reactions in organic synthesis, making it valuable in the development of active pharmaceutical ingredients (APIs). Its fluorinated and brominated structure enhances binding selectivity in bioactive molecules, often exploited in crop protection research and medicinal chemistry for de

Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to the presence of reactive halogen atoms that enable further functionalization. The ester group facilitates coupling reactions in organic synthesis, making it valuable in the development of active pharmaceutical ingredients (APIs). Its fluorinated and brominated structure enhances binding selectivity in bioactive molecules, often exploited in crop protection research and medicinal chemistry for designing novel compounds with improved metabolic stability and potency.

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