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Structure of 2300100-12-1
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This piperidinedione derivative features a 4-methoxybenzyl group that enhances solubility and modulates electronic properties, while the bromo substituent enables downstream functionalization. Bench-stable and compatible with standard synthetic workflows, it serves as a key scaffold in medicinal chemistry for constructing bioactive molecules.
3-Bromo-1-(4-methoxybenzyl)piperidine-2,6-dione serves as a versatile building block for the synthesis of biologically active heterocycles and pharmaceutical intermediates. The molecule combines a bromo-substituted piperidinedione core with a stable 4-methoxybenzyl protecting group, enabling selective functionalization and orthogonal deprotection. Its reactivity supports diverse transformations including nucleophilic substitution, Suzuki coupling, and amide bond formation, making it suitable for medicinal chemistry campaigns requiring modular scaffold elaboration.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H314
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Precautionary Statements : P264-P270-P271-P280-P304+P340-P330-P331-P363-P501
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Lot numbers can be found on the outside label of a product: