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Structure of 1262516-53-9
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This chiral piperidine derivative features a rigid, sterically defined scaffold with two aryl substituents positioned at the α and β carbons, enabling precise stereocontrol in asymmetric synthesis. The (αR,βR) configuration imparts high enantioselectivity in catalytic transformations, particularly in transition-metal-mediated C–C bond formation. Its bench-stable, moisture-tolerant nature simplifies handling under standard conditions.
(αR,βR)-α,β-Diphenyl-1-piperidineethanamine serves as a chiral building block for the synthesis of bioactive molecules, particularly in medicinal chemistry. Its rigid, stereodefined structure enables selective functionalization and facilitates the construction of complex heterocyclic scaffolds. The molecule exhibits good bench stability and compatibility with standard coupling reactions, making it suitable for modular synthesis 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: