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2,3,7,8,12,13,17,18-octaethyl-5,10,15,20-tetraphenylporphyrin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63511-61-5

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63511-61-5 Usage

Chemical compound

2,3,7,8,12,13,17,18-octaethyl-5,10,15,20-tetraphenylporphyrin

Structure

Porphyrin with four substituted phenyl groups and eight ethyl groups attached to the ring

Biological importance

Porphyrins are the active component in heme, which binds oxygen in hemoglobin

Applications

Photodynamic therapy: Can generate reactive oxygen species when exposed to light, leading to destruction of cancerous cells
Organic electronic devices: Potential uses in organic solar cells and organic light-emitting diodes

Research interest

Tetraphenylporphyrin structure is of interest in coordination chemistry and catalysis.

Check Digit Verification of cas no

The CAS Registry Mumber 63511-61-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,5,1 and 1 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 63511-61:
(7*6)+(6*3)+(5*5)+(4*1)+(3*1)+(2*6)+(1*1)=105
105 % 10 = 5
So 63511-61-5 is a valid CAS Registry Number.

63511-61-5Relevant academic research and scientific papers

Effect of ligand nonplanarity and solvent nature on the kinetic stability of zinc porphyrin complexes

Berezin,Shukhto,Shatunov

, p. 997 - 1004 (2008/12/21)

Planarity disturbance in metal porphyrin macrorings produces destabilization of complexes in dimethyl sulfoxide-acetic acid and benzene-acetic acid systems, except for cases where the coordination center is additionally stabilized by endocyclic substituents and/or extra ligands. The first dissociation stage of complexes with N-substituted analogs of porphyrins involves substitution of the acido ligand in the strongly shielded coordination sphere by an electron-donor solvent molecule. The revealed dependences of dissociation rate constants on acid concentration in DMSO, untypical of most metal porphyrins, are explained by a change in the type of the attacking species with changing solvent composition. The dissociation rate constants of complexes in an electron donor solvent can be lower by several orders of magnitude than in a weakly solvating medium.

Microwave-assisted Piloty-Robinson synthesis of 3,4-disubstituted pyrroles

Milgram, Benjamin C.,Eskildsen, Katrine,Richter, Steven M.,Scheidt, W. Robert,Scheidt, Karl A.

, p. 3941 - 3944 (2008/02/01)

(Chemical Equation Presented) The synthesis of N-acyl 3,4-disubstituted pyrroles can be accomplished directly from hydrazine and an aldehyde via a Piloty-Robinson pyrrole synthesis. The use of microwave radiation for the cyclization and pyrrole formation

Phenyl-substituted porphyrins. 1. Synthesis of meso-phenyl-substituted porphyrins

Syrbu,Lyubimova,Semeikin

, p. 1262 - 1270 (2007/10/03)

A method was developed for the synthesis of a series of meso-phenyl-substituted octaalkylporphyrins with various numbers of phenyl groups at various positions. Some of their properties were studied.

Dissociation kinetics of copper and cobalt complexes with sterically distorted porphyrins

Kuvshinova,Kuz'min,Dudkina,Pukhovskaya,Semeikin,Golubchikov

, p. 133 - 136 (2007/10/03)

The dissociation kinetics of the cobalt and copper complexes with octaethylporphyrin, its 5-phenyl, 5,15-diphenyl, and 5,10,15,20-tetraphenyl derivatives, and dodecaphenylporphyrin in acetic acid with small additions of trifluoroacetic acid were studied. In this series of complexes, the steric distortion of the tetrapyrrole macrocycle sequentially increases, which results in a regular decrease in the kinetic stability of the metal porphyrins: The dissociation rate increases by three orders of magnitude.

Kinetics of Complex Formation of Sterically Distorted Porphyrins with Copper Acetate in Pyridine and Dimethylformamide

Dudkina,Shatunov,Kuvshinova,Pukhovskaya,Semeikin,Golubchikov

, p. 1955 - 1960 (2007/10/03)

The kinetics of complex formation of octaethylporphine, 5-monophenyloctaethylporphyrin, 5,15-diphenyloctaethylporphyrin, 5,10,15,20-tetraphenyloctaethylporphyrin, and dodecaphenylporphyrin with copper acetate in pyridine and dimethylformamide was studied.

Synthesis and structural characterization of nonplanar tetraphenylporphyrins with graded degree of β-ethyl substitution

Kalisch, Werner W.,Senge, Mathias O.

, p. 1183 - 1186 (2007/10/03)

Tetraphenylporphyrins bearing two, four, and six β-ethyl groups have been synthesized by mixed condensation of benzaldehyde with diethylpyrrole and pyrrole. Investigation of all isomers by spectroscopy and X-ray crystallography shows a series of porphyrins with graded degree of nonplanarity depending on number and position of the ethyl substituents.

Nonplanar porphyrins. X-ray structures of (2,3,7,8,12,13,17,18-octaethyl- and -octamethyl-5,10,15,20-tetraphenylporphinato)zinc(II)

Barkigia, Kathleen M.,Dolores Berber,Fajer, Jack,Medforth, Craig J.,Renner, Mark W.,Smith, Kevin M.

, p. 8851 - 8857 (2007/10/02)

X-ray structures of the peripherally crowded porphyrins, (2,3,7,8,12,13,17,18-octaethyl-5,10,15,20-tetraphenyl-porphinato)Zn(II)-3MeOH solvate (ZnOETPP-3MeOH) and (2,3,7,8,12,13,17,18-octamethyl-5,10,15,20-tetraphenyl-porphinato)Zn(II)- pyridine-2HCClsub

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