111397-62-7 Usage
Uses
Used in Coordination Chemistry:
3,5-bis(2-benzimidazyl)pyridine is used as a ligand for metal ions in coordination chemistry, leveraging its multiple binding sites to form stable complexes with a variety of metal ions. This property is highly valuable for applications in catalysis, material science, and bioinorganic chemistry.
Used in Catalysis:
In the field of catalysis, 3,5-bis(2-benzimidazyl)pyridine is utilized as a ligand to enhance the catalytic activity of metal ions, improving the efficiency of chemical reactions.
Used in Material Science:
3,5-bis(2-benzimidazyl)pyridine is employed in material science to create new materials with unique properties, such as enhanced stability and reactivity, by forming coordination complexes with metal ions.
Used in Bioinorganic Chemistry:
In bioinorganic chemistry, 3,5-bis(2-benzimidazyl)pyridine is used as a ligand to study the interactions between metal ions and biological systems, contributing to the understanding of metalloenzymes and metalloproteins.
Used in Fluorescence Sensing:
3,5-bis(2-benzimidazyl)pyridine is used in fluorescence sensing applications due to its unique structural and binding properties, allowing for the detection and quantification of specific analytes.
Used in Molecular Recognition:
3，5-bis（2-benzimidazyl）pyridine is utilized in molecular recognition for its ability to selectively bind to certain molecules, which is crucial in the development of sensors and diagnostic tools.
Used in Supramolecular Chemistry:
3,5-bis(2-benzimidazyl)pyridine is applied in supramolecular chemistry to construct complex molecular assemblies and study non-covalent interactions, which is essential for the design of new materials and molecular machines.
Check Digit Verification of cas no
The CAS Registry Mumber 111397-62-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,3,9 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 111397-62:
(8*1)+(7*1)+(6*1)+(5*3)+(4*9)+(3*7)+(2*6)+(1*2)=107
107 % 10 = 7
So 111397-62-7 is a valid CAS Registry Number.
InChI:InChI=1/C19H13N5/c1-2-6-15-14(5-1)21-18(22-15)12-9-13(11-20-10-12)19-23-16-7-3-4-8-17(16)24-19/h1-11H,(H,21,22)(H,23,24)
111397-62-7Relevant articles and documents
Cocrystals and salts of pyridine-3,5-bis(1-methyl-benzimidazole-2-yl) with pyromellitic acid: Aromatic guest inclusion and separation via benzimidazole-carboxylic acid heterosynthon
Dey, Avishek,Bera, Saibal,Biradha, Kumar
, p. 318 - 325 (2015)
An arc-shaped molecule pyridine-3,5-bis(1-methyl-benzimidazole-2-yl) was shown to form cocrystals and salts with pyromellitic acid (H4PMA) which are sustained by COOH?·?·?·Nbim/COO-?·?·?·Hbim heterosynthons. The reaction between these two components in the presence of large aromatic guest molecules resulted in the crystals of salts with aromatic inclusion, while the absence of guests resulted in the H2O and EtOH solvates of cocrystals. The crystal structures of salts exhibited isostructurality with the inclusion of aromatics such as pyrene, perylene, phenanthrene, and 9-anthraldehyde. The crystal structures of solvates were found to differ significantly despite having similar composition. In all these structures the -COOH functional group has exhibited significant preference to interact with the benzimidazole moiety over the pyridine moiety. The aromatic guest inclusion was found to occur via cation?·?·?·?? interactions between the protonated benzimidazole and ??-cloud of guest molecules. The competitive experiments on guest inclusion reveal that the two-component host system exhibits selective inclusion of perylene or 9-anthraldehyde over other aromatics such as pyrene or phenanthrene.
