3-Bromo-5-fluoropyridine

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Reagent Code: #142982
label
Alias 3-Bromo-5-Fluoropyridine
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CAS Number 407-20-5

science Other reagents with same CAS 407-20-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 175.99 g/mol
Formula C₅H₃BrFN
badge Registry Numbers
MDL Number MFCD04112555
thermostat Physical Properties
Melting Point 24-28 °C
Boiling Point 78 °C / 11mmHg
inventory_2 Storage & Handling
Storage Room temperature

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 structure allows for selective functionalization, making it valuable in creating complex nitrogen-containing heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki and Buchwald-Hartwig aminations to build biaryl or arylamine systems found in bioactive molecules. Also utilized in the preparation of kinase inhibitors and other therapeutic agents targeting central nervous system disorders and inflammatory diseases. Its halogen positions enable sequential substitution, offering flexibility in multi-step organic synthesis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿180.00
inventory 5g
10-20 days ฿750.00
inventory 25g
10-20 days ฿2,660.00
inventory 100g
10-20 days ฿10,560.00
inventory 500g
10-20 days ฿47,800.00

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3-Bromo-5-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 structure allows for selective functionalization, making it valuable in creating complex nitrogen-containing heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki and Buchwald-Hartwig aminations to build biaryl or arylamine systems found in bioactive molecules. Also utilized in the preparation of kinase inhibitors

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and active pharmaceutical ingredients (APIs). Its structure allows for selective functionalization, making it valuable in creating complex nitrogen-containing heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki and Buchwald-Hartwig aminations to build biaryl or arylamine systems found in bioactive molecules. Also utilized in the preparation of kinase inhibitors and other therapeutic agents targeting central nervous system disorders and inflammatory diseases. Its halogen positions enable sequential substitution, offering flexibility in multi-step organic synthesis.

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