meso-Tetra (3-pyridyl) porphine

Product Number: T40664; CAS Number: 40882-83-5

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meso-Tetra (3-pyridyl) porphine CAS: 40882-83-5 MDL: MFCD00600955

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Molecular weight: 618.688 g/mol

Molecular Formula: C40H26N8

CAS Number: 40882-83-5

Storage: Store at room temperature, protect from light

Synonyms: 21H,23H-Porphine, 5,10,15,20-tetra-3-pyridinyl-, 5,10,15,20-Tetra(3-pyridinyl)porphyrin, 5,10,15,20-Tetra(3-pyridinyl)porphyrin, 5,10,15,20-Tétra(3-pyridinyl)porphyrine, 5,10,15,20-tetra(3-pyridyl)porphyrin, 5,10,15,20-Tetra(pyridin-3-yl)porphyrin, 40882-83-5, 5,10,15,20-Tetra(3-pyridyl)porphine, 5,10,15,20-Tetra-3-pyridinyl-21H,23H-porphine, 5,10,15,20-Tetrakis(3-pyridyl)porphyrin, 5,10,15,20-tetrapyridin-3-yl-21,22-dihydroporphyrin, AC1L3L8X, AGN-PC-0JMSNY, AGN-PC-0OA834, MCULE-5860596660, meso-Tetra (3-pyridyl) porphine, MFCD00600955, MolPort-000-774-989, SCHEMBL185112, STOCK1N-11837, Tetra(3-pyridyl)porphyrin

Field of Interest: Synthetic Porphyrins, MOF’s, Molecular Recognition, Self Assembly, G-Quadruplex

Background: meso-Tetra (3-pyridyl) porphine is a synthetic porphyrin specialty chemical manufactured by Frontier Specialty Chemicals. meso-Tetra (3-pyridyl) porphine is useful for supramolecular chemistry, G-quadruplex binding, and is a redox active porphyrin.

References:

1.) Lipstman, et al. Versatile Molecular Recognition Features of Tetra(3-pyridyl)porphyrin in Crystal Engineering. Cryst. Growth Des. 2010, 10, 10, 4596–4606. https://doi.org/10.1021/cg1008973

2.) Zakavi, et al. Effects of Core and/or Peripheral Protonation of meso-Tetra(2-, 3-, and 4-pyridyl)Porphyrin and meso-Tetra(3-methylpyridyl)Porphyrin on Their UV-vis Spectra. Journal of Spectroscopy. Volume 2013, Article ID 713745 https://doi.org/10.1155/2013/713745

3.) Martyanov, T.P., Tovstun, S.A., Vasil’ev, S.G. et al. Adsorption of meso-tetra(3-pyridyl)porphyrin on InP/ZnS colloidal quantum dots. J Nanopart Res 24, 129 (2022). https://doi.org/10.1007/s11051-022-05513-4

4.) Choi, et al. An Interdigitated Metalloporphyrin Framework: Two-Dimensional Tessellation, Framework Flexibility, and Selective Guest Accommodation. Cryst. Growth Des. 2010, 10, 1, 171–176. https://doi.org/10.1021/cg900816h

5.) Le, et al. Bcl-2 Promoter Sequence G-Quadruplex Interactions with Three Planar and Non-Planar Cationic Porphyrins: TMPyP4, TMPyP3, and TMPyP2. PLOS ONE. Published: August 20, 2013. https://doi.org/10.1371/journal.pone.0072462

6.) Dutikova, Y.V., Borisova, O.F., Shchyolkina, A.K. et al. 5,10,15,20-Tetra-(N-methyl-3-pyridyl)porphyrin destabilizes the antiparallel telomeric quadruplex d(TTAGGG)4 . Mol Biol 44, 823–831 (2010). https://doi.org/10.1134/S0026893310050201

7.) Dutton, et al. The Influence of Redox-Active Linkers on the Stability and Physical Properties of a Highly Electroactive Porphyrin Nanoprism. Inorg. Chem. 2020, 59, 17, 12616–12624. https://doi.org/10.1021/acs.inorgchem.0c01719

 

Categories

Porphyrins

Scaffold/Subcategory

Synthetic Porphyrins

CAS #

[40882-83-5]

Purity %

>95%

Smiles

N1C2=CC=C1C(C1=CC=CN=C1)=C1C=CC(=N1)/C(C1=CC=CN=C1)=C1NC(/C=C1)=C(C1=NC(C=C1)=C/2C1=CC=CN=C1)C1=CC=CN=C1

Molecular Weight

618.71

Molecular Formula

C40H26N8

Functional Groups

Nitrogen Heterocycle

Porphyrin Family

A4 Porphyrins, Free Base Porphyrins, Tetra-Phenyl Porphine Derivatives

Porphyrin Substitution

Meso-Substituted Porphyrins, Pyridyl Substituted Porphyrins

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