5-Bromo-2-chloro-4-ethoxypyridine

≥95%

Reagent Code: #148121
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CAS Number 52311-48-5

science Other reagents with same CAS 52311-48-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 236.500 g/mol
Formula C₇H₇BrClNO
badge Registry Numbers
MDL Number MFCD21603864
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its halogenated pyridine structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex molecules. Commonly employed in the preparation of agrochemicals and drug candidates requiring specific substitution patterns on the pyridine ring. The presence of bromo and chloro groups enables sequential functionalization, offering flexibility in synthetic routes.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,130.00
inventory 5g
10-20 days ฿10,320.00

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5-Bromo-2-chloro-4-ethoxypyridine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its halogenated pyridine structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex molecules. Commonly employed in the preparation of agrochemicals and drug candidates requiring specific substitution patterns on the pyridine ring. The presence of bromo and chloro groups enables sequential

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its halogenated pyridine structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex molecules. Commonly employed in the preparation of agrochemicals and drug candidates requiring specific substitution patterns on the pyridine ring. The presence of bromo and chloro groups enables sequential functionalization, offering flexibility in synthetic routes.

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