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Structure of 1421052-39-2
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This chiral amide features a (2S)-configured backbone with a diphenylmethyl-protected amine and a sterically hindered trimethylbutanamide moiety. The pendant [(1R,2R)-2-aminocyclohexyl]aminothioxomethyl group imparts unique coordination potential, while the overall structure combines bench-stable handling with precise stereochemical control for use in asymmetric synthesis and peptide mimicry.
(2S)-2-[[[[(1R,2R)-2-Aminocyclohexyl]amino]thioxomethyl]amino]-N-(diphenylmethyl)-N,3,3-trimethylbutanamide serves as a versatile chiral building block for medicinal chemistry campaigns, enabling the synthesis of complex peptidomimetics and heterocyclic scaffolds. Its pendant aminocyclohexyl group provides structural rigidity and stereochemical control, while the diphenylmethyl (DMP) protecting group ensures stability and ease of purification. The thioxomethyl-amino functionality facilitates downstream transformations including cyclization and metal-catalyzed coupling reactions, making it well-suited for iterative synthesis workflows in API 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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: