6-Bromo-2-chloro-3-nitropyridine

96%

Reagent Code: #146309
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CAS Number 1430341-84-6

science Other reagents with same CAS 1430341-84-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 237.44 g/mol
Formula C₅H₂BrClN₂O₂
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 pharmaceutical ingredients (APIs) targeting central nervous system disorders and anti-infective agents. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki and Buchwald-Hartwig aminations to introduce aryl or amine groups. Also utilized in agrochemical research for developing novel pesticides and herbicides due to its electron-deficient pyridine core, which enhances binding to biological targets. Preferred in process chemistry for its reactivity and stability under various reaction conditions.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿580.00
inventory 100mg
10-20 days ฿1,390.00

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6-Bromo-2-chloro-3-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-infective agents. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki and Buchwald-Hartwig aminations to introduce aryl or amine groups. Also utilized in agrochemical research for developing

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-infective agents. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki and Buchwald-Hartwig aminations to introduce aryl or amine groups. Also utilized in agrochemical research for developing novel pesticides and herbicides due to its electron-deficient pyridine core, which enhances binding to biological targets. Preferred in process chemistry for its reactivity and stability under various reaction conditions.

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