5-bromo-2-methoxy-3-nitropyridine

≥95%

Reagent Code: #144171
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CAS Number 152684-30-5

science Other reagents with same CAS 152684-30-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.02 g/mol
Formula C₆H₅BrN₂O₃
badge Registry Numbers
MDL Number MFCD07374968
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in cross-coupling reactions to introduce the pyridine moiety in drug candidates targeting inflammation, cancer, and central nervous system disorders. Also utilized in agrochemical research for the design of novel pesticides due to its electron-deficient ring system that enhances binding to biological targets.

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Test Parameter Specification
Purity (GC) 95-100
Melting point 88-92°C
Appearance Light yellow to gray red-yellow powder

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿144.00
inventory 5g
10-20 days ฿180.00
inventory 25g
10-20 days ฿1,230.00
inventory 100g
10-20 days ฿4,890.00

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5-bromo-2-methoxy-3-nitropyridine
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in cross-coupling reactions to introduce the pyridine moiety in drug candidates targeting inflammation, cancer, and central nervous system disorders. Also utilized in agrochemical research for the

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in cross-coupling reactions to introduce the pyridine moiety in drug candidates targeting inflammation, cancer, and central nervous system disorders. Also utilized in agrochemical research for the design of novel pesticides due to its electron-deficient ring system that enhances binding to biological targets.

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