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Structure of 2897657-05-3
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This sterically encumbered diamine integrates two electron-rich, tert-butyl-substituted aryl units across a central benzene-1,2-diamine core, enabling robust coordination in high-performance organocatalytic systems. The extended π-conjugation and hindered geometry enhance stability and selectivity in asymmetric synthesis applications.
N1-(3',5'-Di-tert-butyl-[1,1'-biphenyl]-2-yl)-N2-(2-(3,5-di-tert-butylphenyl)naphthalen-1-yl)benzene-1,2-diamine serves as a sterically shielded, bench-stable diamine scaffold for the construction of robust transition metal catalysts. Its ortho-di-tert-butyl substitution pattern confers exceptional resistance to oxidative degradation and facilitates clean coordination with late transition metals. The molecule enables efficient formation of chiral ligands and catalytic complexes in asymmetric synthesis, particularly in C–H activation and cross-coupling processes requiring high functional group tolerance and thermal stability.
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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: