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Structure of 67198-21-4
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trans-N,N-Dimethyl-1,2-cyclohexyldiamine features a rigid, stereochemically defined cyclohexane backbone with dimethylamino groups positioned trans to one another. This configuration imparts enhanced steric control and polarity, making the compound well-suited for asymmetric synthesis and as a chiral ligand in transition metal catalysis. The bench-stable, moisture-tolerant nature facilitates straightforward handling in air-sensitive reactions.
trans-N,N-Dimethyl-1,2-cyclohexyldiamine serves as a versatile chiral diamine ligand in asymmetric synthesis, enabling enantioselective transformations through well-established coordination modes. Its bench-stable, sterically defined structure facilitates efficient metal complexation, particularly in palladium- and copper-catalyzed reactions. The dimethyl substitution enhances solubility and functional group tolerance, while the rigid trans-cyclohexane backbone provides predictable stereocontrol—making it a practical choice for scalable catalytic processes and modular scaffold construction.
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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 : H319
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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: