5-Bromo-2-chloro-3-nitropyridine

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Reagent Code: #142977
label
Alias 2-Chloro-3-nitro-5-bromopyridine
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CAS Number 67443-38-3

science Other reagents with same CAS 67443-38-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 237.44 g/mol
Formula C₅H₂BrClN₂O₂
badge Registry Numbers
MDL Number MFCD00222270
thermostat Physical Properties
Melting Point 64-69 °C
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 functional groups allow for selective substitutions, making it valuable in constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki and Buchwald-Hartwig aminations to form carbon-carbon and carbon-nitrogen bonds. Also utilized in agrochemical research for developing novel pesticides and herbicides due to its electron-deficient pyridine core, which enhances binding to biological targets. Suitable for use in material science for designing organic semiconductors and ligands in catalysis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿150.00
inventory 5g
10-20 days ฿168.00
inventory 25g
10-20 days ฿1,100.00
inventory 100g
10-20 days ฿4,200.00

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5-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 functional groups allow for selective substitutions, making it valuable in constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki and Buchwald-Hartwig aminations to form carbon-carbon and carbon-nitrogen bonds. Also utilized in agrochemical resear

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 functional groups allow for selective substitutions, making it valuable in constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki and Buchwald-Hartwig aminations to form carbon-carbon and carbon-nitrogen bonds. Also utilized in agrochemical research for developing novel pesticides and herbicides due to its electron-deficient pyridine core, which enhances binding to biological targets. Suitable for use in material science for designing organic semiconductors and ligands in catalysis.

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