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Structure of 1262411-95-9
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4-Amino-4-methylcyclohexanone hydrochloride features a stable, bench-ready form with enhanced solubility in aqueous and polar organic media. The protonated amine facilitates efficient salt formation, simplifying purification and handling. This cyclic ketone derivative integrates readily into synthetic pathways requiring nitrogen-functionalized ring systems, particularly in medicinal chemistry and asymmetric synthesis applications.
4-Amino-4-methylcyclohexanone hydrochloride serves as a versatile scaffold for medicinal chemistry and asymmetric synthesis. Its amine functionality enables facile derivatization via alkylation, acylation, or reductive amination, while the ketone group supports nucleophilic addition and enolate formation. The hydrochloride salt enhances solubility and stability in aqueous and polar organic media, facilitating purification and handling in standard bench workflows. This compound functions as a key building block in the synthesis of bioactive heterocycles and chiral intermediates.
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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: