5-Bromo-2-hydroxy-4-methylpyridine

97%

Reagent Code: #143486
label
Alias 5-Bromo-4-methyl-2(1H)-pyridone
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CAS Number 164513-38-6

science Other reagents with same CAS 164513-38-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 188.02 g/mol
Formula C₆H₆BrNO
badge Registry Numbers
MDL Number MFCD03427664
thermostat Physical Properties
Melting Point 198-202 °C(lit.)
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 or Buchwald-Hartwig, to introduce aryl or amino groups. Also utilized in agrochemical research for designing new active ingredients due to its stability and reactivity profile.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿180.00
inventory 5g
10-20 days ฿520.00
inventory 25g
10-20 days ฿2,370.00
inventory 100g
10-20 days ฿9,430.00
inventory 500g
10-20 days ฿47,010.00

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5-Bromo-2-hydroxy-4-methylpyridine
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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 or Buchwald-Hartwig, to introduce aryl or amino groups. Also utilized in agrochemical research for designing new active ingredients due to its stability a

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 or Buchwald-Hartwig, to introduce aryl or amino groups. Also utilized in agrochemical research for designing new active ingredients due to its stability and reactivity profile.

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