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Structure of 881386-01-2
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3,3-Dichloro-1-(4-nitrophenyl)piperidin-2-one features a sterically hindered piperidinone core bearing a para-nitro aryl group and two geminal chlorine atoms, conferring enhanced metabolic stability and electron-withdrawing character. This combination enables efficient integration into bioactive scaffolds for medicinal chemistry campaigns requiring lipophilic, electron-deficient heterocycles under standard bench conditions.
3,3-Dichloro-1-(4-nitrophenyl)piperidin-2-one serves as a versatile building block in medicinal chemistry, enabling the synthesis of complex heterocyclic scaffolds through controlled functionalization. Its dichloro substitution at the piperidinone C3 position enhances electrophilicity for nucleophilic displacement, while the para-nitroaryl group provides a handle for reduction or coupling reactions. The compound exhibits bench stability and facilitates straightforward purification, making it suitable for scale-up in API intermediate development.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: