Home Chemistry Heterocyclic Building Blocks Pyrazoles 4,5,6,7-Tetrahydropyrazolo[1,5-A]Pyridine
Acid-Base Reactions: Like many organic compounds, 4,5,6,7-tetrahydropyrazolo[1,5-a]pyridine can undergo acid-base reactions. It can act as either an acid (donating a proton) or a base (accepting a proton) depending on the circumstances.
Nucleophilic Substitution: Depending on the presence of suitable leaving groups or electrophiles, the compound might undergo nucleophilic substitution reactions.
Electrophilic Addition: If there are double or triple bonds present, the compound might undergo electrophilic addition reactions.
Oxidation/Reduction Reactions: Depending on the functional groups present, it might be susceptible to oxidation or reduction reactions.
Cycloaddition Reactions: The structure of 4,5,6,7-tetrahydropyrazolo[1,5-a]pyridine suggests it may participate in cycloaddition reactions.
Metal Complexation: Depending on the reaction conditions, it might be able to coordinate with metal ions.
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4,5,6,7-Tetrahydropyrazolo[1,5-a]pyridine-2-carboxylic acid
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4,5,6,7-Tetrahydropyrazolo[1,5-a]pyridine-3-carbaldehyde
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4,5,6,7-Tetrahydropyrazolo[1,5-a]pyridine-3-carboxylic acid
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3-Chloro-4,5,6,7-tetrahydropyrazolo[1,5-a]pyridine
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4,5,6,7-Tetrahydropyrazolo[1,5-a]pyridine
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Methyl 3-bromo-4,5,6,7-tetrahydropyrazolo[1,5-a]pyridine-2-carboxylate
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