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Structure of 2357109-89-6
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This piperidinedione scaffold integrates a 4-methoxybenzyl group and a hydroxyl substituent, offering enhanced solubility and stability under standard bench conditions. The para-methoxyaryl moiety provides electron-donating character, while the hydroxy function enables downstream derivatization. This structure serves as a key intermediate in the synthesis of bioactive alkaloids and pharmaceutical candidates.
3-Hydroxy-1-(4-methoxybenzyl)piperidine-2,6-dione serves as a versatile building block for heterocyclic synthesis, enabling efficient access to piperidine-based scaffolds via reductive cyclization or functional group manipulation. Its bench-stable nature, combined with orthogonal protection and tolerance to standard reaction conditions, facilitates streamlined workflows in medicinal chemistry and process 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: