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[Fe2O(OCH(CH2N(CH2C5H3(CH3)N)2)2)(O2CC6H5)]2(4+) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

176377-76-7

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176377-76-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 176377-76-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,6,3,7 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 176377-76:
(8*1)+(7*7)+(6*6)+(5*3)+(4*7)+(3*7)+(2*7)+(1*6)=177
177 % 10 = 7
So 176377-76-7 is a valid CAS Registry Number.

176377-76-7Upstream product

176377-76-7Downstream Products

176377-76-7Relevant academic research and scientific papers

Mechanistic Studies of the Formation and Decay of Diiron(III) Peroxo Complexes in the Reaction of Diiron(II) Precursors with Dioxygen

Feig, Andrew L.,Becker, Michael,Schindler, Siegfried,Van Eldik, Rudi,Lippard, Stephen J.

, p. 2590 - 2601 (1996)

Mechanistic studies of the reactions of three analogous alkoxo-bridged diiron(II) complexes with O2 have been carried out. The compounds, which differ primarily in the steric accessibility of dioxygen to the diiron(II) center, form metastable μ-peroxo intermediates when studied at low temperature. At ambient temperatures, these intermediates decay to form (μ-oxo)polyiron(III) products. The effect of ligand steric constraints on the O2 reactivity was investigated. When access to the diiron center was unimpeded, the reaction was first-order with respect to both [Fe2II] and [O2] and the activation parameters for O2 addition were similar to those for O2 reacting with the dioxygen transport protein hemerythrin. When the binding site was occluded, however, reduced order with respect to [O2] was observed and a two-step mechanism was required to explain the kinetic results. Decay of all three peroxide intermediates involves a bimolecular event, implying the formation of tetranuclear species in the transition state.

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