22112-80-7

Usage

Uses

Used in Medical Diagnostics:
4,4',4'',4'''-(21H,23H-Porphine-5,10,15,20-tetrayl)tetrakis(2-methoxyphenol) is utilized as a diagnostic agent for its potential to enhance imaging techniques. 4,4',4'',4'''-(21H,23H-Porphine-5,10,15,20-tetrayl)tetrakis(2-methoxyphenol)'s unique structure and properties may allow for improved detection and monitoring of diseases through techniques such as fluorescence imaging or magnetic resonance imaging (MRI), due to its possible affinity for specific biological targets or its responsiveness to certain stimuli.
Used in Photodynamic Therapy:
In the field of photodynamic therapy, 4,4',4'',4'''-(21H,23H-Porphine-5,10,15,20-tetrayl)tetrakis(2-methoxyphenol) serves as a photosensitizing agent. Its ability to absorb light and generate reactive oxygen species can be harnessed to selectively destroy diseased cells, such as cancer cells, upon exposure to specific wavelengths of light, making it a promising candidate for targeted cancer treatments.
Used as a Building Block for Material Design:
4,4',4'',4'''-(21H,23H-Porphine-5,10,15,20-tetrayl)tetrakis(2-methoxyphenol) is employed as a building block in the design and synthesis of new materials with tailored properties. 4,4',4'',4'''-(21H,23H-Porphine-5,10,15,20-tetrayl)tetrakis(2-methoxyphenol)'s structural features and chemical functionality can be leveraged to create advanced materials for applications in areas such as electronics, optoelectronics, or sensing technologies, where specific characteristics like light absorption, energy transfer, or molecular recognition are required.
Further research and development are necessary to fully explore and understand the potential applications of 4,4',4'',4'''-(21H,23H-Porphine-5,10,15,20-tetrayl)tetrakis(2-methoxyphenol), as its unique structure and properties may lead to innovative uses in various industries.

Upstream product

• 109-97-7 pyrrole 
• 121-33-5 vanillin 

Downstream Products

• 85111-02-0 5,10,15,20-tetrakis(3,4-dihydroxyphenyl)porphyrin 

Relevant academic research and scientific papers

Supercapacitive hybrid materials from the thermolysis of porous coordination nanorods based on a catechol porphyrin

Synthesis of a series of porous coordination polymers with nanorod morphology constructed from a catechol-substituted porphyrin[meso-tetrakis(3,4-dihydroxyphenyl)porphyrin] is reported. While the coordination polymers had moderate surface areas (100-400 m

Synthesis of a Novel Manganese(III) Porphyrin and Its Catalytic Role in Selective Oxidation of Aromatic Alcohols

Abstract: A novel azido complex of manganese(III) porphyrin with 1-methylimidazole has been synthesized. This complex can be abbreviated as [MnIII(THMPP)N3(1-MeIm)], where THMPP is 5,10,15,20-tetrakis(4-hydroxy-3-methoxyphenyl)porphi

Synthesis and characterization of free base and metal porphyrins and their interaction with CdTe QDs

Free base porphyrins and metalloporphyrins with different number of methoxy groups were synthesized to investigate the consequence of methoxy groups in the porphyrins on interaction with quantum dots through steady state, time resolved and transient absor

Some novel manganese(III) porphyrins with catalytic properties

A series of manganese(III) porphyrins with?4-methylimidazole have been prepared. These are high-spin complexes having general formula [MnIII(THMPP)X(4-MeIm)], where THMP = 5,10,15,20-tetra(4-hydroxy-3-methoxyphenyl)porphine ligand, X = Cl?

One-flask synthesis of porphyrin metal complexes

One-flask synthesis of metallo porphyrins by condensation of aromatic aldehydes with pyrrole in refluxing propionic acid in presence of corresponding metal acetates is described. The yields are better when compared to Rothemund and Adler-Longo methods.

The synthesis of new potential photosensitizers

Abstract Several new derivatives of tetrakis(hydroxyphenyl)porphyrin were synthesized and their physicochemical data were established. These data were further assessed in terms of the synthesized compounds' usefulness as potential photosensitizers in anticancer photodynamic therapy. Absorption and fluorescence spectra, as well as triplet state lifetime were determined along with the compounds' stability and capacity to generate singlet oxygen. They obtained were compared to the corresponding data pertaining to a well-known and clinically admitted photosensitizing drug (Foscan).

Porphyrin synthesis in surfactant solution: Multicomponent assembly in micelles

A synthesis of meso-substituted porphyrins in anionic sodium dodecyl sulfate micelles has been developed. Polar, functionalized aromatic aldehydes condense reversibly with pyrrole in the micellar phase. Oxidation of the porphyrinogen then provides functionalized porphyrins in yields of 10-48%. Hydrophobic aldehydes condense irreversibly to give low yields at practical substrate concentrations. Synthesis in D2O solution results in per-β-deuterated porphyrins. A two-phase model is used to rationalize the dependence of porphyrin yield on reactant and surfactant concentration. Micelles are viewed as potential wells which promote porphyrinogen assembly by binding products more tightly than reactants.