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Phosphonic acid, phenyl-, cerium(4+) salt (2:1) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75406-80-3

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75406-80-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75406-80-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,4,0 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 75406-80:
(7*7)+(6*5)+(5*4)+(4*0)+(3*6)+(2*8)+(1*0)=133
133 % 10 = 3
So 75406-80-3 is a valid CAS Registry Number.

75406-80-3Upstream product

75406-80-3Downstream Products

75406-80-3Relevant academic research and scientific papers

Cerium(IV) phenylphosphonates and para-substituted phenylphosphonates: preparation and characterization

Melánová,Bene?,Svoboda,Zima,Trchová,Vl?ek,Almonasy

, p. 331 - 339 (2017)

Cerium(IV) phenylphosphonates and 4-substituted phenylphosphonates were prepared by reaction of a cerium(IV) salt with corresponding acids (phenylphosphonic, 4-carboxyphenylphosphonic, 4-sulfamoylphenylphosphonic, 1,4-benzenediphosphonic, 1,4-biphenyldiphosphonic and 4-sulfophenylphosphonic acid) and characterized by elemental analysis, energy-dispersive X-ray analysis, TGA, powder X-ray diffraction and infrared spectroscopy. Three different cerium phenylphosphonates can be prepared in dependence on the reaction conditions. On the other hand, only one compound is formed in each 4-substituted phosphonate system regardless the variation of the reaction conditions. All three phenylphosphonates, 4-carboxyphenylphosphonate and 4-sulfamoylphenylphosphonate are layered with the organic parts pointed below and above the plane of the metal phosphonate layers, with the functional groups placed at the end of the organic part. 4-Sulfophenylphosphonate, 1,4-benzenediphosphonate and 4,4′-biphenyldiphosphonate form pillared structures. Cerium 4-carboxyphenylphosphonate is able to intercalate aliphatic amines due to the presence of the free carboxylic groups in its interlayer space.

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