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Structure of 2640520-10-9
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This chiral diamine features two trifluoromethylphenyl groups flanking a stereodefined ethane backbone, delivering enhanced electron density and steric bulk. The N1,N2-dimethyl substitution improves solubility and reduces undesired coordination while maintaining configurational stability. Designed for asymmetric synthesis applications, this scaffold enables precise stereocontrol in transition metal catalysis and ligand development.
(1S,2S)-N1,N2-Dimethyl-1,2-bis(4-(trifluoromethyl)phenyl)ethane-1,2-diamine serves as a chiral diamine scaffold with enhanced steric and electronic properties derived from the trifluoromethyl aryl groups. Its bench-stable nature and defined stereochemistry facilitate reliable use in asymmetric catalysis, particularly in transition-metal-catalyzed transformations. The molecule exhibits good functional group tolerance and enables efficient formation of chiral complexes for enantioselective synthesis.
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GHS Pictogram :
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GHS No : GHS09
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Signal Word : Danger
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UN#: 3082
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Class : 9
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Packing Group : Ⅲ
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Hazard Statements : H410
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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: