Fe(III) meso-Tetra(4-methoxyphenyl) porphine chloride

Product Number: T40527; CAS Number: 36995-20-7

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Fe(III) meso-Tetra(4-methoxyphenyl) porphine chloride CAS: 36995-20-7 MDL: MFCD00012405

Molecular weight: 824.12 g/mol

Molecular Formula: C48H36ClFeN4O4

CAS Number: 36995-20-7

Storage: Store at room temperature, protect from light

Synonyms: 36995-20-7, Chlor[5,10,15,20-tetrakis(4-methoxyphenyl)porphyrinato(2-)-κ2N21,N23]eisen, Chloro[5,10,15,20-tetrakis(4-methoxyphenyl)porphyrinato(2-)-κ2N21,N23]iron, Chloro[5,10,15,20-tétrakis(4-méthoxyphényl)porphyrineato(2-)-κ2N21,N23]fer, Iron, chloro[5,10,15,20-tetrakis(4-methoxyphenyl)-21H,23H-porphinato(2-)-κN21,κN23]-, MFCD00012405, 5,10,15,20-TETRAKIS -21H,23H-PORPHINEIRON CHLORIDE,  5,10,15,20-TETRAKIS(4-METHOXYPHENYL)-21H,23H-PORPHINE IRON(III) CHLORIDE, 5,10,15,20-TETRAKIS(4-METHOXYPHENYL)-21H,23H-PORPHINEIRON(III)CHLORIDE, Fe(III) meso-Tetra(4-methoxyphenyl) porphine chloride

Fields of Interest: Synthetic Porphyrins, Iron Porphyrins, Catalysis, Cyclopropanation, Proton Coupled Electron Transfer (PCET)

Background: Fe(III) meso-Tetra(4-methoxyphenyl) porphine chloride is a synthetic porphyrin derivative manufactured by Frontier Specialty Chemicals. Fe(III) meso-Tetra(4-methoxyphenyl) porphine chloride is useful for numerous catalytic transformations of organic and small molecules.1-6

References:   

1.) Wolf, et al. Shape and stereoselective cyclopropanation of alkenes catalyzed by iron porphyrins. J. Am. Chem. Soc. 1995, 117, 36, 9194–9199. https://doi.org/10.1021/ja00141a011

2.) Baumann, et al. Iron Porphyrin Catalyzed N−H Insertion Reactions with Ethyl Diazoacetate. Organometallics 2007, 26, 16, 3995–4002. https://doi.org/10.1021/om0610997

3.) Guo, et al. A new evidence of the high-valent oxo–metal radical cation intermediate and hydrogen radical abstract mechanism in hydrocarbon hydroxylation catalyzed by metalloporphyrins. Journal of Molecular Catalysis A: Chemical. Volume 157, Issues 1–2, 20 June 2000, Pages 31-40. https://doi.org/10.1016/S1381-1169(99)00444-6

4.) Wang, et al. A Green Process for Oxidation of p-Nitrotoluene Catalyzed by Metalloporphyrins under Mild Conditions. Org. Process Res. Dev. 2006, 10, 4, 757–761. https://doi.org/10.1021/op060056z

5.) Gericke, et al. Oxo-Free Hydrocarbon Oxidation by an Iron(III)-Isoporphyrin Complex. Inorg. Chem. 2020, 59, 19, 13952–13961. https://doi.org/10.1021/acs.inorgchem.0c01618

6.) Lu, et al. Dioxygen reduction catalyzed by substituted iron tetraphenylporphyrins in acidic media. Journal of Porphyrins and Phthalocyanines. Vol. 16, No. 03, pp. 310-315 (2012). https://doi.org/10.1142/S1088424612500356

Categories

Porphyrins

Scaffold/Subcategory

Synthetic Porphyrins

CAS #

[36995-20-7]

Purity %

>95%

Smiles

COC1=CC=C(C=C1)C1=C2C=CC(=N2)/C(=C2/C=CC3=C(C4=NC(C=C4)=C(/C4=CC=C1N4[Fe](Cl)N23)C1=CC=C(OC)C=C1)C1=CC=C(OC)C=C1)C1=CC=C(OC)C=C1

Molecular Weight

824.122

Molecular Formula

C48H36ClFeN4O4

Functional Groups

Alkoxy, Methoxy

Porphyrin Family

A4 Porphyrins, Metallo Porphyrins, Tetra-Phenyl Porphine Derivatives

Porphyrin Substitution

Meso-Substituted Porphyrins, Pyridyl Substituted Porphyrins

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