Introduction of CAS:14945-24-5 | 5,10,15,20-TETRA(4-DIMETHYLAMINOPHENYL)PORPHYRIN
The synthesis of porphyrin derivatives often involves multi-step organic reactions, aiming at incorporating functional groups that modify the compound's physical, chemical, or photophysical properties. For instance, the Pictet-Spengler synthesis has been applied to incorporate nitrogenous heterocyclic scaffolds into porphyrins, enhancing their π-conjugation and improving biological, optical, and electrochemical properties.
Specification of CAS:14945-24-5 | 5,10,15,20-TETRA(4-DIMETHYLAMINOPHENYL)PORPHYRIN
|
ITEMS |
SPECIFICATION |
|
CAS |
14945-24-5 |
|
Molecular Formula |
C52H50N8 |
|
Density |
1.225±0.06 g/cm3(Predicted) |
|
Purity |
98% |
Research Application of CAS:14945-24-5 | 5,10,15,20-TETRA(4-DIMETHYLAMINOPHENYL)PORPHYRIN
Cationic Porphyrins in Water: Kano, Takei, and Hashimoto (1990) studied the intermolecular interactions of cationic porphyrins in water, focusing on fluorescence behavior and dimer formation (Kano, Takei, & Hashimoto, 1990).
Optical Nonlinearity of Polyaniline−Porphyrin Nanocomposite: Pandey, Sandeep, Philip, and Lakshminarayanan (2009) observed enhanced optical limiting properties in a nanocomposite of polyaniline and a porphyrin derivative, offering potential applications in optical devices (Pandey, Sandeep, Philip, & Lakshminarayanan, 2009).
Emission Spectroscopic Properties in Chemiluminescence Systems: Staninski, Kaczmarek, Lis, and Elbanowski (2003) investigated water-soluble porphyrins in chemiluminescence systems with different metal ions, highlighting their potential in analytical chemistry (Staninski, Kaczmarek, Lis, & Elbanowski, 2003).
Fluorescence Quenching by Xanthine Compounds: Makarska-Białokoz (2015) studied the interaction of water-soluble porphyrins with xanthine compounds, finding significant fluorescence quenching effects, relevant for biochemical studies (Makarska-Białokoz, 2015).
Interaction with PAMAM Dendrimers: Kubát, Lang, and Zelinger (2007) explored how anionic and cationic porphyrins bind to PAMAM dendrimers, which could have implications in drug delivery and materials science (Kubát, Lang, & Zelinger, 2007).
Photodegradation of Phenols: Monteiro et al. (2005) utilized water-soluble porphyrinic compounds as sensitizers for photodegrading phenols, indicating their use in environmental remediation (Monteiro et al., 2005).
Corrosion Inhibition in Steel: Singh et al. (2017) studied the effectiveness of heterocyclic porphyrin compounds in inhibiting corrosion in steel, showing potential in material protection (Singh, Talha, Xu, Sun, & Lin, 2017).
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