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Structure of 1638137-85-5
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This bench-stable, moisture-tolerant compound features a chiral piperazinone core with a methyl-substituted nitrogen, enabling efficient integration into medicinal chemistry libraries. The hydrochloride salt enhances solubility and handling, facilitating direct use in synthesis workflows without additional purification.
(S)-1-(3-Methylpiperazin-1-yl)ethanone hydrochloride serves as a versatile chiral building block in medicinal chemistry, enabling the synthesis of piperazinyl-containing scaffolds prevalent in bioactive molecules. The protected amine functionality offers compatibility with standard coupling reactions and facilitates downstream derivatization. Its crystalline solid form ensures bench stability and ease of handling, while the hydrochloride salt enhances solubility in polar solvents, streamlining purification and reaction setup in routine synthetic workflows.
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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: