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Structure of 58520-03-9
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This chiral diamine features two 4'-methoxyphenyl groups flanking a rigid ethane backbone, enabling precise spatial control in asymmetric synthesis. The para-methoxy substituents enhance solubility and electronic modulation, while the (1R,2R) stereochemistry ensures high enantioselectivity in transition metal complexation. Ideal for catalyst design in stereoselective transformations.
(1R,2R)-1,2-Di(4'-methoxyphenyl)-1,2-diaminoethane serves as a chiral diamine building block for asymmetric catalysis and ligand development. Its rigid, enantiomerically pure structure enables precise stereocontrol in transition-metal-catalyzed reactions. The methoxy-substituted aryl groups enhance solubility and electronic tuning, while the diamine functionality offers robust coordination to metals such as Pd, Ni, and Cu. Bench-stable and readily purified by standard techniques, it functions effectively in established asymmetric synthesis workflows.
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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: