2-bromo-5-methoxy-4-nitropyridine

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Reagent Code: #141683
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CAS Number 1805513-34-1

science Other reagents with same CAS 1805513-34-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.0195 g/mol
Formula C₆H₅BrN₂O₃
badge Registry Numbers
MDL Number MFCD28741609
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active ingredients for drugs targeting central nervous system disorders and antimicrobial agents. Its structure allows for selective functionalization, making it valuable in creating complex pyridine-based molecules. Commonly employed in cross-coupling reactions to build biaryl systems in medicinal chemistry. Also utilized in agrochemical research for developing new crop protection agents due to its reactivity and stability in multi-step syntheses.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,600.00
inventory 250mg
10-20 days ฿16,000.00
inventory 1g
10-20 days ฿32,000.00
inventory 5g
10-20 days ฿80,000.00

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2-bromo-5-methoxy-4-nitropyridine
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active ingredients for drugs targeting central nervous system disorders and antimicrobial agents. Its structure allows for selective functionalization, making it valuable in creating complex pyridine-based molecules. Commonly employed in cross-coupling reactions to build biaryl systems in medicinal chemistry. Also utilized in agrochemical research for developing new crop protection agents due to its reactivity

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active ingredients for drugs targeting central nervous system disorders and antimicrobial agents. Its structure allows for selective functionalization, making it valuable in creating complex pyridine-based molecules. Commonly employed in cross-coupling reactions to build biaryl systems in medicinal chemistry. Also utilized in agrochemical research for developing new crop protection agents due to its reactivity and stability in multi-step syntheses.

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