2-halopyridines
2-Halopyridines are a class of organic compounds that belong to the pyridine series, featuring an aromatic six-membered ring with one halogen atom (commonly bromine or chlorine) attached at the 2-position. These compounds play crucial roles in various chemical reactions and have applications in pharmaceuticals, pesticides, and as intermediates in the synthesis of other organic molecules.
The presence of a halogen group enhances their reactivity and can significantly influence their physical properties such as solubility, melting point, and boiling point. For instance, 2-chloropyridine exhibits a lower melting point compared to its parent compound pyridine due to weaker intermolecular forces.
In pharmaceutical research, 2-halopyridines are often used as building blocks for developing novel drug candidates targeting various biological pathways. Their unique structural features make them valuable in the design of selective inhibitors and agonists. Additionally, these compounds are also explored for their potential as herbicides and insecticides due to their inherent toxicity towards certain pests.
The versatility of 2-halopyridines makes them indispensable tools in organic synthesis, offering diverse reactivity patterns that can be exploited depending on the desired outcome of the reaction sequence.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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2-(6-bromopyridin-3-yl)acetaldehyde | 722535-98-0 | C7H6BrNO |
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6-fluoro-3-hydroxypyridine-2-carbonitrile | 727736-71-2 | C6H3FN2O |
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2-Fluoro isonornicotine | 1270485-14-7 | C9H11FN2 |
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5-(chloromethyl)-2-fluoropyridine | 315180-15-5 | C6H5ClFN |
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(6-fluoropyridin-2-yl)methanol | 315180-17-7 | C6H6FNO |
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2-Chloro-6-methylpyridin-3-ol | 35680-24-1 | C6H6ClNO |
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2-chloro-5-(1H-imidazol-4-yl)pyridine | 790262-70-3 | C8H6ClN3 |
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5-(N-Boc-Aminomethyl)-2-Bromopyridine | 864266-29-5 | C11H15BrN2O2 |
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3-(6-Bromo-pyridin-2-Yl)-isoxazol-5-ylamine | 887595-06-4 | C8H6BrN3O |
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2-bromo-5-(3-bromopropyl)pyridine | 918145-48-9 | C8H9Br2N |
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