5-Bromo-2-fluoronicotinic acid

98%

Reagent Code: #151316
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CAS Number 29241-66-5

science Other reagents with same CAS 29241-66-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 220.00 g/mol
Formula C₆H₃BrFNO₂
badge Registry Numbers
MDL Number MFCD06797939
thermostat Physical Properties
Boiling Point 327.4 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

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 structure allows for selective functionalization, making it valuable in medicinal chemistry for creating compounds with high target specificity. Commonly employed in cross-coupling reactions such as Suzuki-Miyaura and Buchwald-Hartwig aminations to build complex heterocyclic systems. Also utilized in agrochemical research for designing new active ingredients with improved metabolic stability and binding affinity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿340.00
inventory 5g
10-20 days ฿1,070.00
inventory 25g
10-20 days ฿5,020.00

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5-Bromo-2-fluoronicotinic acid
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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 structure allows for selective functionalization, making it valuable in medicinal chemistry for creating compounds with high target specificity. Commonly employed in cross-coupling reactions such as Suzuki-Miyaura and Buchwald-Hartwig aminations to build complex heterocyclic systems. Also utilized in agrochemical research for designing new active ingredie

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating compounds with high target specificity. Commonly employed in cross-coupling reactions such as Suzuki-Miyaura and Buchwald-Hartwig aminations to build complex heterocyclic systems. Also utilized in agrochemical research for designing new active ingredients with improved metabolic stability and binding affinity.

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