3-Bromo-5-Acetylpyridine

99%

Reagent Code: #143771
label
Alias 3-bromo-5-acetylpyridine; 3-acetyl-5-bromopyridine, 3-acetyl-5-bromopyridine
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CAS Number 38940-62-4

science Other reagents with same CAS 38940-62-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.03 g/mol
Formula C₇H₆BrNO
badge Registry Numbers
MDL Number MFCD03086033
thermostat Physical Properties
Melting Point 77-79°C
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 nicotinic receptor modulators and drugs targeting neurological disorders. Its structure allows for selective functionalization, making it valuable in creating active pharmaceutical ingredients (APIs) with high specificity. Commonly employed in cross-coupling reactions, such as Suzuki and Heck reactions, to build complex pyridine-based molecules. Also utilized in agrochemicals for designing novel pesticides and herbicides due to its bioactive scaffold. Its versatility in heterocyclic chemistry supports research in medicinal chemistry and drug discovery.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿247.50
inventory 5g
10-20 days ฿1,910.00
inventory 25g
10-20 days ฿7,820.00

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3-Bromo-5-Acetylpyridine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators and drugs targeting neurological disorders. Its structure allows for selective functionalization, making it valuable in creating active pharmaceutical ingredients (APIs) with high specificity. Commonly employed in cross-coupling reactions, such as Suzuki and Heck reactions, to build complex pyridine-based molecules. Also utilized in agrochemicals for designing novel pesticides

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor modulators and drugs targeting neurological disorders. Its structure allows for selective functionalization, making it valuable in creating active pharmaceutical ingredients (APIs) with high specificity. Commonly employed in cross-coupling reactions, such as Suzuki and Heck reactions, to build complex pyridine-based molecules. Also utilized in agrochemicals for designing novel pesticides and herbicides due to its bioactive scaffold. Its versatility in heterocyclic chemistry supports research in medicinal chemistry and drug discovery.

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