Home Chemistry Heterocyclic Building Blocks Piperidines (E)-N-(3-Oxo-1-Phenyl-3-(Piperidin-1-Yl)Prop-1-En-2-Yl)Benzamide
Aldol Reaction: The enone functionality in the compound can participate in an aldol reaction, forming new carbon-carbon bonds.
Amide Hydrolysis: Under acidic or basic conditions, the amide bond can undergo hydrolysis to yield the corresponding carboxylic acid and amine.
Wittig Reaction: The compound can undergo a Wittig reaction with a suitable phosphonium ylide to form an olefin.
Reduction: The ketone functionality can be reduced to an alcohol using reducing agents like sodium borohydride or lithium aluminum hydride.
Grignard Reaction: The compound can react with a Grignard reagent to form a new carbon-carbon bond.
Oxidation: The compound can undergo oxidation reactions, such as with mild oxidizing agents like Jones reagent, to convert the alcohol or alkene functionality into higher oxidation states.
Heterocycle Formation: The compound can be used as a starting material for the synthesis of various heterocyclic compounds, depending on the reaction conditions and reagents used.
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(Z)-N-(1-(4-Bromophenyl)-1-chloro-3-oxo-3-(piperidin-1-yl)prop-1-en-2-yl)benzamide
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(Z)-N-(1-Chloro-3-oxo-3-(piperidin-1-yl)-1-(o-tolyl)prop-1-en-2-yl)benzamide
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(Z)-N-(1-Chloro-3-oxo-1-phenyl-3-(piperidin-1-yl)prop-1-en-2-yl)benzamide
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(Z)-N-(1-Chloro-1-(4-methoxyphenyl)-3-oxo-3-(piperidin-1-yl)prop-1-en-2-yl)benzamide
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(Z)-N-(1-Chloro-3-oxo-3-(piperidin-1-yl)-1-(p-tolyl)prop-1-en-2-yl)benzamide
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(Z)-N-(1-Chloro-1-(2-fluorophenyl)-3-oxo-3-(piperidin-1-yl)prop-1-en-2-yl)benzamide
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