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Structure of 53152-69-5
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This chiral diamine features a rigid cyclohexane backbone with stereospecific methyl groups at the 1 and 2 positions, enabling precise stereocontrol in asymmetric synthesis. The N-methyl substitution enhances solubility and stability while minimizing unwanted coordination sites. Ideal for ligand design in transition metal catalysis and as a building block in enantioselective transformations.
(1R,2R)-N1,N1,N2,N2-Tetramethylcyclohexane-1,2-diamine serves as a chiral diamine ligand in asymmetric catalysis, enabling high enantioselectivity in transition metal-catalyzed reactions. Its rigid cyclohexane backbone and sterically defined methyl groups enhance stereocontrol, while the bench-stable, crystalline nature facilitates handling and purification. Functions effectively in copper- and palladium-mediated transformations, particularly in conjugate additions and C–C bond formations.
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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: