876905-57-6

Basic information

• Product Name: 3,5-di(pyridin-4-yl)phenol
• Synonyms: 3,5-di(pyridin-4-yl)phenol
• CAS NO: 876905-57-6
• Molecular Formula: C₁₆H₁₂N₂O
• Molecular Weight: 248.27928
• Mol File: 876905-57-6.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3,5-di(pyridin-4-yl)phenol(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-di(pyridin-4-yl)phenol(876905-57-6)
• EPA Substance Registry System: 3,5-di(pyridin-4-yl)phenol(876905-57-6)

Safety Data

• Hazardous Substances Data: 876905-57-6(Hazardous Substances Data)

Usage

Uses

Used in Chelating Applications:
3,5-di(pyridin-4-yl)phenol is used as a chelating agent for its ability to form stable complexes with metal ions. This property is valuable in various chemical processes and analytical techniques, where the selective binding of metal ions can facilitate reactions or enhance the detection of specific elements.
Used in Pharmaceutical and Biochemical Research:
3,5-di(pyridin-4-yl)phenol is used as a potential therapeutic agent due to its antitumor and antioxidant properties. Its ability to interact with biological systems and modulate cellular processes makes it a candidate for further research into the development of new drugs and treatments for various diseases.
Used in Analytical Chemistry:
3,5-di(pyridin-4-yl)phenol is used as a fluorescent probe in analytical chemistry. Its strong fluorescence allows for the sensitive detection and quantification of various analytes, making it a valuable tool in the development of new analytical methods and techniques.
Used in Bioimaging Applications:
3,5-di(pyridin-4-yl)phenol is used as a fluorescent marker in bioimaging. Its ability to bind to specific biological targets and emit light upon excitation makes it useful for visualizing cellular structures, tracking molecular interactions, and studying biological processes in living organisms.

Upstream product

• 1692-15-5 4-pyridylboronic acid 
• 626-41-5 3,5-dibromophenol 
• 181219-01-2 4-pyridineboronic acid pinacol ester 
• 74137-36-3 3,5-dibromoanisole 
• 1352646-02-6 4,4'-(5-methoxy-1,3-phenylene)dipyridine 

Downstream Products

• 1352646-03-7 2-(2-(2-(3,5-di(pyridin-4-yl)phenoxy)ethoxy)ethoxy)ethanol 
• 1416767-36-6 C₂₁H₁₄N₂O₂S 
• 1416767-37-7 C₂₁H₁₄N₂O₂S 

Relevant articles and documents

Amphipathic rhombic supramolecular metal macrocycle as well as preparation method and application thereof (by machine translation)

The invention discloses an amphipathic rhombic supramolecular metal macrocyclic compound as well as a preparation method and application thereof. The structure of the amphipathic rhombic supramolecular metal macrocyclic compound is shown as a formula (I). The preparation method of the amphipathic rhombic supramolecular metal macrocyclic compound comprises the following steps: mixing a glucose group-modified 120°-bipyridine ligand L and a methoxy functionalized 60°-diplatinum receptor A and the like, and forming an amphipathic rhombic supramolecular metal macrocyclic compound by self-assembly of the orientation coordinate bonds between the two Pt (II)- N. The invention further provides a preparation of the amphipathic rhombic supramolecular metal macrocyclic compound Use of a vector. (by machine translation)

Hierarchical Gelation of a Pd12L24 Metal-Organic Cage Regulated by Cholesteryl Groups

The creation of supramolecular assemblies by assembly of structurally simple components via supramolecular interactions provides an opportunity to develop functional materials with hierarchical complexibility. Herein, we report an assembly approach to supramolecular gels based on metal-organic cages with tunable hierarchical structures and properties. A Pd12L24 cage (L is cholesteryl-functionalized 3,5-bis(4-pyridyl)benzene) bearing 24 cholesteryl groups is used as a supramolecular building unit and molecular platform for functionalization with tunable functional behaviors. The Pd12L24 cage motifs spontaneously self-assemble into gels where orthogonal metal-organic coordination and cholesteryl-cholesteryl interactions are involved in the gelation. The Pd12L24 cage exhibits a reversible transition between solution and aggregated gel states in response to temperature. The gelation and the mechanical property are rarely regulated by deuterated solvents and tetramethylsilane. The mechanical property of the gel materials is tunable by varying the content of cholesteryl groups of Pd12L24. Functional moieties (e.g., luminescent TPE group) can be introduced on the cage, and the luminescent property changes while the structure is maintained. The Pd12L24 gel shows visible anion-responsive behaviors arising from the hierarchical structure.

Thiophene-coated functionalized M12L24 spheres: Synthesis, characterization, and electrochemical properties

Instant balls: Well-defined thiophene-coated functional nanospheres were synthesized by instantaneous self-assembly of twelve 90° Pd II-containing compounds and twenty-four 120° organic bidentate ligands in acetone. This solvent system was efficient to prepare the self-assembled complexes, facilitating isolation and purification. The self-assembled functional nanospheres exhibited interesting electrochemical properties. Copyright

A sphere-in-sphere complex by orthogonal self-assembly

Russian dolls: Two covalently tethered, curved bispyridinyl ligands and PdII ions have been shown to self-assemble into a sphere-in-sphere complex (6.3 nm in diameter; see X-ray structure). The two ligands did not form heteroleptic mixed complexes, but instead assembled into two distinct homogeneous [M12L24] cuboctahedra, reminiscent of a double-shell viral capsid. Copyright