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Structure of 70708-33-7
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This chiral diamine dihydrochloride features a rigid cyclohexane backbone with defined (1R,2R) stereochemistry, enabling precise asymmetric induction. The dimethyl substitution enhances solubility and steric control, while the paired ammonium chloride salts ensure stability and ease of handling in catalytic and synthetic applications.
(1R,2R)-N1,N2-Dimethylcyclohexane-1,2-diamine dihydrochloride serves as a chiral diamine scaffold enabling asymmetric synthesis in transition metal catalysis. Its rigid, enantiopure cyclohexane backbone provides predictable stereocontrol in ligand design, while the N-methyl groups enhance solubility and reduce basicity for improved handling. Functions effectively in Pd- and Cu-catalyzed cross-couplings and C–H functionalizations, offering bench-stable, easily purified intermediates with high reproducibility in multigram-scale applications.
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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: