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Structure of 894493-95-9
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This chiral diamine features a rigid cyclohexane backbone with stereodefined (1S,2S) configuration, enabling precise control in asymmetric synthesis. The N1,N1-dimethyl substitution enhances solubility and steric shielding, while the secondary amine sites facilitate coordination in catalytic systems. Ideal for ligand design and enantioselective transformations.
(1S,2S)-N1,N1-Dimethylcyclohexane-1,2-diamine serves as a chiral diamine scaffold in asymmetric synthesis, enabling stereoselective catalysis through well-defined coordination to transition metals. Its bench-stable, crystalline form facilitates handling and purification, while the N1,N1-dimethyl substitution enhances solubility and resistance to oxidation. Functions effectively in enantioselective hydrogenation, C–C coupling, and metal-ligand complex formation, offering broad compatibility with common reaction conditions.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 2735
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H314-H318
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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: