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Structure of 2444430-73-1
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This chiral diamine features two 2-chlorophenyl groups positioned on a rigid ethylene backbone, enabling precise stereocontrol in asymmetric synthesis. The dimethyl substitution enhances solubility and stability, while the ortho-chloro substituents provide strong electronic modulation and steric influence. Ideal for coordinating transition metals in catalytic systems requiring defined chiral environments.
(1R,2R)-1,2-Bis(2-chlorophenyl)-N1,N2-dimethylethane-1,2-diamine serves as a chiral diamine scaffold for asymmetric catalysis, enabling enantioselective transformations in transition-metal-mediated reactions. Its rigid, sterically defined structure facilitates high diastereocontrol in C–C and C–heteroatom bond formations. The ortho-chlorophenyl groups enhance π-stacking interactions and improve catalyst stability, while the N-methyl substituents reduce basicity and minimize side coordination, improving functional group tolerance and simplifying purification in 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: