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Structure of 320778-92-5
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This chiral diamine features a rigid 1,2-diamino scaffold with defined stereochemistry at both ring carbons. The N1,N1-dimethyl substitution enhances solubility and steric shielding, while the cyclohexane backbone provides conformational stability. It serves as a modular ligand in asymmetric catalysis and functional building block for bioactive molecule synthesis.
(1R,2R)-N1,N1-Dimethylcyclohexane-1,2-diamine serves as a chiral diamine scaffold enabling asymmetric catalysis and ligand design. Its rigid cyclohexane backbone provides defined stereochemistry for enantioselective transformations, while the N1,N1-dimethyl substitution enhances solubility and reduces basicity, facilitating handling and purification. Functions effectively in transition metal-catalyzed reactions and as a building block for bioactive heterocycles.
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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: