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Structure of 2697181-89-6
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This chiral bis-imidazole features two (S)-sec-butyl groups and sterically shielded tert-butylphenyl substituents, delivering enhanced stability and solubility in organic media. The rigid, C₂-symmetric scaffold enables precise spatial control in asymmetric catalysis and molecular recognition applications.
(4S,4'S)-4,4'-Di((S)-sec-butyl)-1,1'-bis(3-(tert-butyl)phenyl)-4,4',5,5'-tetrahydro-1H,1'H-2,2'-biimidazole serves as a sterically encumbered, chiral bis-imidazole ligand designed for transition-metal catalysis. Its robust bench stability and orthogonal functional group tolerance enable reliable coordination in Pd- or Ni-catalyzed cross-coupling reactions. The (S)-sec-butyl and tert-butyl substituents provide enhanced stereochemical control and prevent undesired aggregation, facilitating efficient catalyst turnover and purification in asymmetric synthesis workflows.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: