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Structure of 58520-04-0
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This chiral diamine features two 4'-methoxyphenyl groups flanking a rigid ethylene backbone, enabling precise spatial control in asymmetric synthesis. The para-methoxy substituents enhance solubility and electronic modulation, while the (1S,2S) stereochemistry ensures high enantioselectivity in transition metal complexation. Ideal for ligand design in catalytic transformations requiring defined chiral environments.
(1S,2S)-1,2-Di(4'-methoxyphenyl)-1,2-diaminoethane serves as a chiral diamine building block for asymmetric catalysis and ligand design. Its two methoxy-substituted aryl groups provide enhanced solubility and steric definition, while the rigid (1S,2S)-configuration enables precise stereocontrol in transition metal complexes. The molecule exhibits good bench stability and facilitates efficient coordination to metals such as Pd, Cu, and Ni, making it valuable in cross-coupling and enantioselective transformations.
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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: