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Structure of 1462921-50-1
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This bench-stable ketone features a 3-aminoazetidinyl moiety that integrates readily into bioactive molecule scaffolds. The hydrochloride salt enhances solubility and handling, enabling efficient coupling under standard conditions for medicinal chemistry applications.
1-(3-Aminoazetidin-1-yl)ethanone hydrochloride serves as a versatile building block for medicinal chemistry, enabling the rapid construction of nitrogen-containing heterocycles. The azetidine core offers enhanced metabolic stability and improved membrane permeability in bioactive molecules. Its amine functionality facilitates straightforward derivatization via acylation, alkylation, or coupling reactions, while the hydrochloride salt ensures excellent bench stability and ease of handling. This compound functions as a key intermediate in the synthesis of kinase inhibitors and other pharmaceutical scaffolds.
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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: