Home Chemistry Heterocyclic Building Blocks Pyrazoles 2-Phenyl-2,4-Dihydro-3H-Pyrazol-3-One
Aldol Condensation: It can undergo aldol condensation reactions with aldehydes or ketones in the presence of a base to form β-diketones.
Hydrazine Reaction: It can react with hydrazine or its derivatives to form hydrazones. This reaction is often used for the identification of carbonyl compounds.
Reduction: The carbonyl group can be reduced to the corresponding alcohol using reducing agents like sodium borohydride or lithium aluminum hydride.
Acylation: It can undergo acylation reactions with acyl chlorides or anhydrides in the presence of a Lewis acid catalyst to introduce acyl groups.
Halogenation: It can be halogenated at the α-carbon atom by treatment with appropriate halogenating agents like bromine or chlorine.
Cyclization Reactions: It can participate in various cyclization reactions to form heterocyclic compounds when combined with other reagents.
Grignard Reaction: When treated with a Grignard reagent, it can undergo nucleophilic addition reactions to form tertiary alcohols.
Oxidation: It can be oxidized to the corresponding carboxylic acid using strong oxidizing agents like potassium permanganate or chromic acid.
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4-(3-Methyl-5-oxo-4,5-dihydro-1H-pyrazol-1-yl)benzenesulfonic acid
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4-Chloro-3-(3-methyl-5-oxo-4,5-dihydro-1H-pyrazol-1-yl)benzenesulfonic acid
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2,5-Dichloro-4-(3-methyl-5-oxo-4,5-dihydro-1H-pyrazol-1-yl)benzenesulfonic acid
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2-(2-Chlorophenyl)-5-methyl-2,4-dihydro-3H-pyrazol-3-one
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1-(3,4-Dimethylphenyl)-3-methyl-1H-pyrazol-5(4H)-one
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1-Phenyl-3-(trifluoromethyl)-1H-pyrazol-5(4H)-one
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5-Oxo-1-(4-sulfophenyl)-4,5-dihydro-1H-pyrazole-3-carboxylic acid
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Deoxycytidine triphosphate trisodium salt
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5'-Deoxy-5-fluoro-N-[(pentyloxy)carbonyl]cytidine 2',3'-diacetate
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