2-bromo-4-methyl-5-nitropyridine

≥95%

Reagent Code: #144191
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CAS Number 23056-47-5

science Other reagents with same CAS 23056-47-5

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Weight 217.02 g/mol
Formula C₆H₅BrN₂O₂
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MDL Number MFCD03095066
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Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) targeting central nervous system disorders and anti-inflammatory agents. It serves as a building block in agrochemicals for creating herbicides and fungicides due to its reactivity in cross-coupling reactions. Commonly employed in research laboratories for constructing complex pyridine-based molecules, especially in medicinal chemistry for drug discovery. Its nitro and bromo functional groups allow selective modifications, enabling the introduction of various substituents through nucleophilic substitution or metal-catalyzed reactions.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿2,310.00
inventory 100g
10-20 days ฿8,630.00
inventory 500g
10-20 days ฿41,600.00

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2-bromo-4-methyl-5-nitropyridine
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) targeting central nervous system disorders and anti-inflammatory agents. It serves as a building block in agrochemicals for creating herbicides and fungicides due to its reactivity in cross-coupling reactions. Commonly employed in research laboratories for constructing complex pyridine-based molecules, especially in medicinal chemistry for drug discovery. Its nitro and

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) targeting central nervous system disorders and anti-inflammatory agents. It serves as a building block in agrochemicals for creating herbicides and fungicides due to its reactivity in cross-coupling reactions. Commonly employed in research laboratories for constructing complex pyridine-based molecules, especially in medicinal chemistry for drug discovery. Its nitro and bromo functional groups allow selective modifications, enabling the introduction of various substituents through nucleophilic substitution or metal-catalyzed reactions.

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