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Based on the provided literature, **10,15,20-tris<2,6-bis(pivaloyloxy)phenyl>-20-<(2-hydroxy-6-pivaloyloxy)phenyl>porphyrin** is a synthetic porphyrin derivative featuring a sterically hindered structure with multiple pivaloyloxy groups on the phenyl substituents, creating a "bis-fenced" or double-pocketed geometry around the porphyrin core. This design facilitates selective ligand binding, particularly for dioxygen or axial imidazole coordination in its iron(II) complex form, making it relevant for biomimetic studies of heme proteins. The hydroxyl group at the 20-position further contributes to its functional versatility.

130203-62-2

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130203-62-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 130203-62-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,2,0 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 130203-62:
(8*1)+(7*3)+(6*0)+(5*2)+(4*0)+(3*3)+(2*6)+(1*2)=62
62 % 10 = 2
So 130203-62-2 is a valid CAS Registry Number.

130203-62-2Downstream Products

130203-62-2Relevant academic research and scientific papers

Synthesis and Dioxygen-binding Properties of Double-sided Porphyrinatoiron(II) Complexes bearing Covalently Bound Axial Imidazole

Tsuchida, Eishun,Komatsu, Teruyuki,Arai, Kenji,Nishide, Hiroyuki

, p. 2465 - 2469 (1993)

Double-sided porphyrinatoiron(II) complexes bearing covalently bound axial imidazole, 5--10,15,20-trisporphyrinatoiron(II) and 5-2-(3,3-dimethylbutyryloxy)-6-(5-imidazolylvaler

A Bis-Fenced Porphinatoiron Having Seven Pivaloyloxy Groups on the Porphyrin Ring Plane. Synthesis and Ligand Binding

Tsuchida, Eishun,Hasegawa, Etsuo,Komatsu, Teruyuki,Nakao, Keisuke,Nishide, Hiroyuki

, p. 1071 - 1074 (1990)

A new tetraphenylporphyrin derivative having two pockets on both sides of the porphyrin ring plane, 5,10,15-tri(2',6'-bis(pivaloyloxy)phenyl)-20-((2'-hydroxy-6'-pivaloyloxy)phenyl)porphine, and its iron complex were synthesized.The 1,2-dimethylimidazole b

Synthesis and Coordination Behaviors of New Double-Sided Porphyrinatoiron(II) Complexes: Effect of the Pocket-Size for Imidazole on Dioxygen Binding

Tsuchida, Eishun,Hasegawa, Etsuo,Komatsu, Teruyuki,Nakata, Taisaku

, p. 888 - 894 (2007/10/02)

The synthesis and characteristic ligation behaviors of new "double-sided porphyrinatoiron(II) complexes" having two pockets of different spacing-size on each side of a ring plane and a larger sized one on both sides of a macrocycle, are described.The equilibrium constants for the imidazole derivatives to the four-coordinated porphyrinatoiron(II)s were increased in proportion to the size of the pocket-space, which is reflected by the ΔH term.The five-coordinated complexes of the porphyrinatoirons, obtained by the addition of 1,2-dimethylimidazole (1,2-dmim) in a toluene solution, formed stable and reversible dioxygen adducts at 25 deg.The oxygen affinities for the iron(II) complexes increased as the steric bulk on the rear side of the porphyrin plane was relieved.These changes in the oxygen affinity are attributed to the strength of the ?-electron donation from the imidazole to the central iron ion.

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