3-Iodo-2-nitropyridine

98%

Reagent Code: #199752
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CAS Number 54231-34-4

science Other reagents with same CAS 54231-34-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 249.99 g/mol
Formula C₅H₃IN₂O₂
thermostat Physical Properties
Boiling Point 336.6°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of pyridine-based active ingredients. Its structure, featuring iodo and nitro groups at positions 3 and 2, allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions to introduce the pyridine moiety in drug candidates. Also utilized in research settings for the preparation of nitropyridine derivatives with potential biological activity, including reductions of the nitro group to amines for further synthetic steps.

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inventory 1g
10-20 days ฿660.00

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3-Iodo-2-nitropyridine
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of pyridine-based active ingredients. Its structure, featuring iodo and nitro groups at positions 3 and 2, allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions to introduce the pyridine moiety in drug candidates. Also utilized in research settings for the preparation of nit

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of pyridine-based active ingredients. Its structure, featuring iodo and nitro groups at positions 3 and 2, allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions to introduce the pyridine moiety in drug candidates. Also utilized in research settings for the preparation of nitropyridine derivatives with potential biological activity, including reductions of the nitro group to amines for further synthetic steps.

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