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Structure of 135822-72-9
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This bipyridine derivative features two aldehyde groups positioned at the 5 and 5′-sites, enabling precise coordination in metal-ligand assemblies. The electron-deficient pyridine rings enhance binding affinity for transition metals, while the aldehyde functionalities facilitate post-modification via reductive amination or hydrazone formation. Ideal for constructing redox-active scaffolds in catalysis and molecular sensing applications.
[2,2'-Bipyridine]-5,5'-dicarboxaldehyde serves as a versatile bifunctional building block in coordination chemistry and catalysis. Its two aldehyde groups enable facile imine formation and derivatization, while the rigid bipyridine core provides strong metal-chelating capability. The molecule exhibits excellent bench stability and compatibility with standard synthetic protocols, facilitating the construction of functionalized ligands, porous materials, and redox-active scaffolds for applications in homogeneous catalysis and molecular electronics.
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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: