5-bromo-4-methylpyridine-2-carboxylic acid

≥95%

Reagent Code: #143999
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CAS Number 886365-02-2

science Other reagents with same CAS 886365-02-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.03 g/mol
Formula C₇H₆BrNO₂
badge Registry Numbers
MDL Number MFCD07375100
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 kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki and Buchwald-Hartwig aminations to form carbon-carbon and carbon-nitrogen bonds. Also utilized in agrochemical research for designing new active ingredients due to its stability and reactivity profile.

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Test Parameter Specification
Purity 95-100
Appearance SOLID

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿490.00
inventory 5g
10-20 days ฿2,050.00

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5-bromo-4-methylpyridine-2-carboxylic 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 constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki and Buchwald-Hartwig aminations to form carbon-carbon and carbon-nitrogen bonds. Also utilized in agrochemical research for designing new active ingredient

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 constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki and Buchwald-Hartwig aminations to form carbon-carbon and carbon-nitrogen bonds. Also utilized in agrochemical research for designing new active ingredients due to its stability and reactivity profile.

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