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α,β,α,β-5,10,15,20-tetrakisporphyrin is a complex organic compound that belongs to the class of porphyrins. Porphyrins are large heterocyclic macrocycles with a central metal ion, and they are known for their ability to absorb light, making them important in various biological processes such as photosynthesis and respiration. This specific porphyrin derivative features four phenylalanine-based substituents attached to the porphyrin core, with each phenylalanine residue being protected by a t-butoxycarbonyl (Boc) group. The Boc protection is commonly used in peptide synthesis to prevent unwanted side reactions. The compound's structure is characterized by its symmetrical arrangement of substituents, with each of the four phenyl groups being attached at the ortho position relative to the porphyrin core. This particular porphyrin is of interest in chemical and materials science due to its potential applications in areas such as catalysis, sensing, and photovoltaics, where its light-harvesting properties and chemical reactivity can be exploited.

97419-33-5

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97419-33-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97419-33-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,4,1 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 97419-33:
(7*9)+(6*7)+(5*4)+(4*1)+(3*9)+(2*3)+(1*3)=165
165 % 10 = 5
So 97419-33-5 is a valid CAS Registry Number.

97419-33-5Relevant academic research and scientific papers

Asymmetric Epoxidation of Alkenes catalysed by a 'Basket-handle' Iron-Porphyrin bearing Amino Acids

Mansuy, D.,Battioni, P.,Renaud, J.-P.,Guerin, P.

, p. 155 - 156 (1985)

A 'basket-handle' iron-porphyrin bearing L-phenylalanine residues has been prepared and found to catalyse the epoxidation of p-chlorostyrene with a 50percent excess of the (R)-epoxide, whereas 'picket' iron-porphyrins bearing the same amino acid have led

Chiral basket-handle porphyrin-Co complexes for the catalyzed asymmetric cycloaddition of CO2 to epoxides

Fu, Xiying,Jing, Xinyao,Jin, Lili,Zhang, Lilong,Zhang, Xiaofeng,Hu, Bin,Jing, Huanwang

, p. 997 - 1003 (2018/05/23)

The catalytic synthesis of cyclic carbonates via the cycloaddition of CO2 to epoxides is a standard methodology for CO2 fixation. For this purpose, chiral basket-handle porphyrin-Co complexes were devised, prepared, and fully characterized by nuclear magnetic resonance, mass spectrometry, Fourier transform infrared spectroscopy, ultraviolet-visible spectroscopy, and specific rotation. The proposed metalloporphyrin catalysts were synthesized with either 1,1′-bi-2-naphthol or L-phenylalanine, which have different chirality, and then applied to the coupling of propylene oxide and CO2 for generating chiral cyclic carbonates with good enantioselectivity under extremely mild conditions in the presence of tetrabutyl ammonium chloride as a co-catalyst. The good enantioselectivity in the cycloaddition reaction is attributed to a synergistic interplay between the chiral porphyrin catalysts and the substrate. The mechanism and enantioselectivity of the asymmetric cycloaddition reaction is discussed.

Both-faces Hindered Porphyrins. Part 5. 1 Synthesis and Characterization of Iron(III) Basket Handle Porphyrins having Multiple Secondary Amide Groups inserted in the Superstructures

Maillard, Philippe,Schaeffer, Corinne,Huel, Christiane,Lhoste, Jean-Marc,Momenteau, Michel

, p. 3285 - 3296 (2007/10/02)

The synthesis of basket handle porphyrins in a cross-trans configuration (27) and (28) derived from 5,10,15,20-tetrakis (o-aminophenyl)porphyrin, and their hydroxy-iron(III) complexes, in which one of the faces is hindered by a bridge substituted by one o

CONDENSATION D'ACIDES AMINES SUR DES MESO-AMINO-2-PHENYL PORPHYRINES

Lecas, Alexandra,Renko, Zafiarisoa,Rose, Eric

, p. 1019 - 1022 (2007/10/02)

The condensation of aminoacids on meso-tetra-(2-aminophenyl) and meso-α,γ-bis-(2,6-diaminophenyl)porphyrins is reported.

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