Cas no 56396-12-4 (meso-Tetra(2,4,6-trimethylphenyl)porphine)
meso-Tetra(2,4,6-trimethylphenyl)porphine Chemical and Physical Properties
Names and Identifiers
-
- 5,10,15,20-Tetrakis(2,4,6-trimethylphenyl)-21H,23H-porphine
- meso-Tetra(2,4,6-trimethylphenyl)porphine
- 2,7,12,17-Tetrakis(2,4,6-trimethylphenyl)-21,22,23,24-tetraazapentacyclo[16.2.1.1,6.18,.1,6]tetracosa-1,3,5,7,9,11(23),12,14,16,18(21),19-undecaene
- 5,10,15,20-tetrakis(2,4,6-trimethylphenyl)-21,22-dihydroporphyrin
- 5,10,15,20-Tetrakis(2,4,6-trimethylphenyl)porphyrin
- T72626
- SCHEMBL949016
- (5Z,10Z,14Z,19Z)-5,10,15,20-tetrakis(2,4,6-trimethylphenyl)-21,23-dihydroporphyrin
- 2,7,12,17-tetrakis(2,4,6-trimethylphenyl)-21,22,23,24-tetraazapentacyclo[16.2.1.1(3),6.18,(1)(1).1(1)(3),(1)6]tetracosa-1,3,5,7,9,11(23),12,14,16,18(21),19-undecaene
- T1729
- 2,7,12,17-tetrakis(2,4,6-trimethylphenyl)-21,22,23,24-tetraazapentacyclo[16.2.1.1^{3,6}.1^{8,11}.1^{13,16}]tetracosa-1,3,5,7,9,11(23),12,14,16,18(21),19-undecaene
- tetramesitylporphyrin
- 5,10,15,20-tetrakis(2,4,6-trimethylphenyl)-21,23-dihydroporphyrin
- CS-0086077
- Q27123346
- Tetrakistrimethylphenylporphin
- 56396-12-4
- meso-tetra(2,4,6-trimethylphenyl)porphyrin
- AKOS025394752
- AKOS015842212
- A869958
- DL-0709
- CHEBI:52278
- MFCD01321200
- KBIOUJDBIXSYJT-UHFFFAOYSA-N
- 5,10,15,20-Tetrakis(2,4,6-trimethylphenyl)-21H,23H-porphin
- DB-306279
-
- MDL: MFCD01321200
- Inchi: 1S/C56H54N4/c1-29-21-33(5)49(34(6)22-29)53-41-13-15-43(57-41)54(50-35(7)23-30(2)24-36(50)8)45-17-19-47(59-45)56(52-39(11)27-32(4)28-40(52)12)48-20-18-46(60-48)55(44-16-14-42(53)58-44)51-37(9)25-31(3)26-38(51)10/h13-28,57,60H,1-12H3/b53-41+,53-42+,54-43+,54-45+,55-44+,55-46+,56-47+,56-48+
- InChI Key: KBIOUJDBIXSYJT-RNWYWIMESA-N
- SMILES: N1C2C=CC1=C(C1C=CC(=C(C3C(C)=CC(C)=CC=3C)C3=CC=C(C(=C4C=CC(C=2C2C(C)=CC(C)=CC=2C)=N4)C2C(C)=CC(C)=CC=2C)N3)N=1)C1C(C)=CC(C)=CC=1C |c:5,10,31,t:26|
Computed Properties
- Exact Mass: 782.43500
- Monoisotopic Mass: 782.435
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 60
- Rotatable Bond Count: 4
- Complexity: 1290
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Surface Charge: 0
- Tautomer Count: 2
- XLogP3: 14.8
- Topological Polar Surface Area: 57.4A^2
Experimental Properties
- Density: 1.142
- Refractive Index: 1.639
- PSA: 56.30000
- LogP: 10.56700
meso-Tetra(2,4,6-trimethylphenyl)porphine Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | T162694-1G |
meso-Tetra(2,4,6-trimethylphenyl)porphine |
56396-12-4 | 98% | 1g |
¥5470.90 | 2023-08-31 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | T162694-100MG |
meso-Tetra(2,4,6-trimethylphenyl)porphine |
56396-12-4 | 98% | 100mg |
¥881.90 | 2023-08-31 | |
| Chemenu | CM203515-1g |
5,10,15,20-Tetrakis(2,4,6-trimethylphenyl)porphyrin |
56396-12-4 | 95% | 1g |
$638 | 2021-08-04 | |
| TI XI AI ( SHANG HAI ) HUA CHENG GONG YE FA ZHAN Co., Ltd. | T1729-1G |
5,10,15,20-Tetrakis(2,4,6-trimethylphenyl)porphyrin |
56396-12-4 | >98.0%(HPLC) | 1g |
¥3550.00 | 2024-04-16 | |
| Alichem | A019123311-1g |
5,10,15,20-Tetrakis(2,4,6-trimethylphenyl)porphyrin |
56396-12-4 | 95% | 1g |
$695.64 | 2023-09-01 | |
| Frontier Specialty Chemicals | T972-100 mg |
meso-Tetra(2,4,6-trimethylphenyl)porphine |
56396-12-4 | 100mg |
$ 41.00 | 2022-11-04 | ||
| Frontier Specialty Chemicals | T972-250 mg |
meso-Tetra(2,4,6-trimethylphenyl)porphine |
56396-12-4 | 250mg |
$ 84.00 | 2022-11-04 | ||
| Frontier Specialty Chemicals | T972-1 g |
meso-Tetra(2,4,6-trimethylphenyl)porphine |
56396-12-4 | 1g |
$ 284.00 | 2022-11-04 | ||
| Frontier Specialty Chemicals | T972-500 mg |
meso-Tetra(2,4,6-trimethylphenyl)porphine |
56396-12-4 | 500mg |
$ 158.00 | 2022-11-04 | ||
| Chemenu | CM203515-1g |
5,10,15,20-Tetrakis(2,4,6-trimethylphenyl)porphyrin |
56396-12-4 | 95% | 1g |
$*** | 2023-05-30 |
meso-Tetra(2,4,6-trimethylphenyl)porphine Suppliers
meso-Tetra(2,4,6-trimethylphenyl)porphine Related Literature
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Inna A. Abdulaeva,Kirill P. Birin,Julien Michalak,Anthony Romieu,Christine Stern,Alla Bessmertnykh-Lemeune,Roger Guilard,Yulia G. Gorbunova,Aslan Yu. Tsivadze New J. Chem. 2016 40 5758
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2. Axial ligand exchange of iron(III) tetramesitylporphyrin phenolate complexesMichael W. Nee,John R. Lindsay Smith J. Chem. Soc. Dalton Trans. 1999 3373
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3. Reactivity of ruthenium 5,10,15,20-tetramesitylporphyrin towards diazoesters: formation of olefinsJ. P. Collman,E. Rose,G. D. Venburg J. Chem. Soc. Chem. Commun. 1993 934
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Tse-Hong Chen,Nawras Asiri,Ka Wai Kwong,Jonathan Malone,Rui Zhang Chem. Commun. 2015 51 9949
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Tse-Hong Chen,Nawras Asiri,Ka Wai Kwong,Jonathan Malone,Rui Zhang Chem. Commun. 2015 51 9949
Additional information on meso-Tetra(2,4,6-trimethylphenyl)porphine
Meso-Tetra(2,4,6-trimethylphenyl)porphine and Its Applications in Modern Chemical Biology
Meso-Tetra(2,4,6-trimethylphenyl)porphine, a compound with the CAS number 56396-12-4, is a highly versatile and synthetically accessible porphyrin derivative. This compound has garnered significant attention in the field of chemical biology due to its unique structural and electronic properties. Porphyrins, as a class of macrocyclic compounds, are known for their extensive applications in various biological and chemical processes. The introduction of bulky substituents such as 2,4,6-trimethylphenyl groups into the porphyrin core enhances its stability and functionality, making it an attractive candidate for numerous applications.
The synthesis of Meso-Tetra(2,4,6-trimethylphenyl)porphine involves a series of well-established organic reactions, including the condensation of meso-dipyrromethanes with appropriate substituents. The presence of methyl groups at the 2,4,6 positions not only imparts steric hindrance but also influences the electronic environment of the porphyrin ring. This modification is crucial for tuning its photophysical and redox properties, which are essential for its utility in various biochemical assays and therapeutic applications.
One of the most compelling aspects of Meso-Tetra(2,4,6-trimethylphenyl)porphine is its ability to act as a photosensitizer. In recent years, there has been a surge in research focusing on photodynamic therapy (PDT) as an effective treatment modality for various diseases. The compound's high molar extinction coefficient and favorable excited-state properties make it an excellent candidate for generating singlet oxygen upon light irradiation. This reactive oxygen species (ROS) can selectively target and destroy cancer cells while minimizing damage to healthy tissues.
Recent studies have demonstrated the potential of Meso-Tetra(2,4,6-trimethylphenyl)porphine in combating drug-resistant tumors. By incorporating this porphyrin derivative into nanocarriers or conjugating it with targeting ligands, researchers have been able to enhance its specificity and efficacy. For instance, a study published in the journal Nature Materials reported the development of porphyrin-based nanocapsules that selectively deliver payloads to tumor sites, significantly improving treatment outcomes.
Beyond its applications in medicine, Meso-Tetra(2,4,6-trimethylphenyl)porphine has found utility in environmental science and catalysis. Its ability to absorb visible light makes it an ideal candidate for photocatalytic systems designed to degrade organic pollutants. Additionally, the compound's redox-active nature has been exploited in designing molecular wires and sensors for detecting trace amounts of analytes.
The development of new synthetic methodologies has further expanded the scope of Meso-Tetra(2,4,6-trimethylphenyl)porphine. Advances in metal-catalyzed cross-coupling reactions have enabled the introduction of diverse functional groups onto the porphyrin core, opening up possibilities for tailored applications. For example, researchers have successfully synthesized porphyrins with pendant groups that can participate in host-guest interactions or form metal complexes with unique properties.
In conclusion, Meso-Tetra(2,4,6-trimethylphenyl)porphine (CAS number 56396-12-4) is a remarkable compound with broad applications in chemical biology and beyond. Its unique structural features and tunable properties make it an invaluable tool for researchers working on photodynamic therapy, drug delivery systems, environmental remediation, and catalysis. As synthetic chemistry continues to evolve, it is likely that even more innovative uses for this compound will be discovered.
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