Home Chemistry Heterocyclic Building Blocks Pyrazoles 1-(Tetrahydro-2H-Pyran-2-Yl)-1H-Pyrazole
Substitution reactions: If there are suitable leaving groups in the molecule (e.g., halogens or other good leaving groups), substitution reactions (e.g., SN1 or SN2) can occur at those sites.
Ring-opening reactions: The tetrahydro-2H-pyran ring in the molecule could potentially undergo ring-opening reactions under specific conditions, such as with acid or base catalysis.
Addition reactions: Depending on the reaction conditions and the reagents used, addition reactions might occur at various positions in the molecule.
Oxidation or reduction reactions: The presence of heteroatoms like oxygen and nitrogen in the molecule makes it susceptible to oxidation or reduction reactions, depending on the reagents and conditions used.
Condensation reactions: It may undergo condensation reactions with suitable reagents to form larger or more complex molecules.
Rearrangements: Depending on the conditions, intramolecular or intermolecular rearrangements could take place.
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5-Bromo-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazole
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(1-(Tetrahydro-2H-pyran-2-yl)-1H-pyrazol-4-yl)methanamine
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4-Bromo-5-nitro-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazole
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(1-(Tetrahydro-2H-pyran-2-yl)-1H-pyrazol-4-yl)methanol
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4-Bromo-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazole
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3-Bromo-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazole
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5-Iodo-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazole
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4-Iodo-1-(tetrahydropyran-2-yl)-1H-pyrazole
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