2-Bromo-5-chloro-3-fluoropyridine

98%

Reagent Code: #144992
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CAS Number 514797-97-8

science Other reagents with same CAS 514797-97-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 210.43 g/mol
Formula C₅H₂BrClFN
badge Registry Numbers
MDL Number MFCD11044268
thermostat Physical Properties
Boiling Point 190.8°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and active pharmaceutical ingredients (APIs). Its halogen substituents allow for selective cross-coupling reactions, making it valuable in building complex molecules through palladium-catalyzed reactions like Suzuki or Heck couplings. Commonly employed in the production of herbicides, fungicides, and certain kinase inhibitors in medicinal chemistry. Its structure supports fine-tuning of electronic and steric properties in drug design.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿174.00
inventory 5g
10-20 days ฿500.00
inventory 25g
10-20 days ฿1,890.00
inventory 100g
10-20 days ฿7,510.00
inventory 500g
10-20 days ฿37,530.00

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2-Bromo-5-chloro-3-fluoropyridine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and active pharmaceutical ingredients (APIs). Its halogen substituents allow for selective cross-coupling reactions, making it valuable in building complex molecules through palladium-catalyzed reactions like Suzuki or Heck couplings. Commonly employed in the production of herbicides, fungicides, and certain kinase inhibitors in medicinal chemistry. Its structure supports fine-tuning of electr

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and active pharmaceutical ingredients (APIs). Its halogen substituents allow for selective cross-coupling reactions, making it valuable in building complex molecules through palladium-catalyzed reactions like Suzuki or Heck couplings. Commonly employed in the production of herbicides, fungicides, and certain kinase inhibitors in medicinal chemistry. Its structure supports fine-tuning of electronic and steric properties in drug design.

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