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Structure of 143443-23-6
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This chiral diamine features two benzyl-protected amine groups on a rigid cyclohexane backbone, enabling precise stereocontrol in asymmetric synthesis. The (1R,2R) configuration ensures high enantioselectivity when used as a ligand or auxiliary in transition-metal-catalyzed reactions. Bench-stable and moisture-tolerant, it integrates seamlessly into catalytic systems requiring defined spatial orientation and robust handling under standard conditions.
(1R,2R)-N,N'-Bis(phenylmethyl)-1,2-cyclohexanediamine serves as a chiral diamine ligand in asymmetric catalysis, enabling enantioselective transformations through well-defined coordination geometries. Its rigid cyclohexane backbone and benzylic N-protecting groups confer excellent bench stability and ease of purification. The molecule functions effectively in transition metal-catalyzed reactions, particularly in hydrogenation and C–C bond-forming processes, offering high enantioselectivity and reproducible results across standard 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: