Home Chemistry Heterocyclic Building Blocks Pyrroles (Z)-3-((1H-Pyrrol-2-Yl)Methylene)Indolin-2-One
Aldol Condensation: The compound can undergo aldol condensation reactions with itself or other suitable carbonyl compounds in the presence of a base, leading to the formation of β-unsaturated carbonyl compounds.
Michael Addition: It can participate in Michael addition reactions with nucleophiles, such as amines or thiols, at the β-carbon, which is the carbon next to the carbonyl group.
Reduction: The carbonyl group can be reduced to the corresponding alcohol using reducing agents like sodium borohydride or lithium aluminum hydride.
Cyclization: Depending on the reaction conditions, it may undergo intramolecular cyclization reactions to form heterocyclic compounds.
Hydrolysis: The compound can undergo hydrolysis under acidic or basic conditions to cleave the molecule at the carbonyl group, forming carboxylic acids or their salts.
Oxidation: It can be oxidized using oxidizing agents to convert the indolinone moiety to various oxidation states.
Halogenation: The compound can be halogenated at various positions, depending on the reaction conditions and the choice of halogenating agent.
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(Z)-5-((5-Fluoro-2-oxoindolin-3-ylidene)methyl)-2,4-dimethyl-1H-pyrrole-3-carboxylic acid
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