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Structure of 29176-55-4
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2,9-Dichloro-1,10-phenanthroline features two chlorine substituents at the 2 and 9 positions of the phenanthroline scaffold, enhancing electron-withdrawing character and improving metal-chelation stability. This bench-stable ligand integrates readily into coordination complexes for catalytic applications and redox studies.
2,9-Dichloro-1,10-phenanthroline serves as a versatile ligand in transition metal catalysis, particularly in palladium-catalyzed cross-coupling reactions. Its electron-withdrawing dichloro substituents enhance oxidative stability and modulate redox potential, enabling efficient catalytic cycles. The rigid aromatic scaffold provides strong chelation to metal centers, facilitating catalyst formation and improving selectivity in C–C and C–heteroatom bond constructions. This compound exhibits excellent bench stability and is compatible with diverse functional groups, making it a practical choice for synthetic applications requiring robust ligand performance.
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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: