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chloro(5,10,15,20-tetrakis(2-chloro-6-fluoro-3-sulfonatophenyl)porphyrinato)iron(III) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

834856-83-6

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834856-83-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 834856-83-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,3,4,8,5 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 834856-83:
(8*8)+(7*3)+(6*4)+(5*8)+(4*5)+(3*6)+(2*8)+(1*3)=206
206 % 10 = 6
So 834856-83-6 is a valid CAS Registry Number.

834856-83-6Downstream Products

834856-83-6Relevant academic research and scientific papers

Catalytic activity of anionic iron(III) porphyrins immobilized on grafted disordered silica obtained from acidic leached chrysotile

Halma, Matilte,Bail, Alesandro,Wypych, Fernando,Nakagaki, Shirley

, p. 44 - 51 (2006)

Hydrated disordered silica obtained by leaching chrysotile with hydrochloric acid was grafted with 3-APTS and reacted with aqueous iron porphyrins solutions of [Fe(TDFSPP) and Fe(TCFSPP)]. The obtained materials were characterized by powder X-ray diffraction (PXRD), UV-vis, FTIR and electron paramagnetic resonance (EPR) spectroscopies and investigated as catalysts in oxidation reaction of cyclohexane using iodosylbenzene as oxidant. The catalytic activities obtained in heterogeneous media for Fe(TDFSPP) was superior to the results obtained in homogeneous conditions but the opposite effect was observed for the Fe(TCFSPP), indicating that instead of the structural similarity of both iron porphyrins (second generation porphyrins), the immobilization way produced different catalysts. The best catalytic activity of the Fe(TDFSPP)/Si-3-APTS (65%) compared to Fe(TCFSPP)/Si-3-APTS (33%) can be explained by the easy access of the oxidant and the substrate to the catalytic sites in the former. A schematic representation for the immobilization and a mechanism for the oxidation reaction have been presented.

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