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dimethyl ester of benzophenonetetracyclic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

47587-11-1

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47587-11-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 47587-11-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,7,5,8 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 47587-11:
(7*4)+(6*7)+(5*5)+(4*8)+(3*7)+(2*1)+(1*1)=151
151 % 10 = 1
So 47587-11-1 is a valid CAS Registry Number.

47587-11-1Downstream Products

47587-11-1Relevant academic research and scientific papers

Influence of the molecular structure of H complexes of dialkyl dihydrogen benzophenonetetracarboxylates with aromatic diamines on the viscosity of their melts

Artem'eva,Baklagina,Kukarkina,Kostereva,Samarin,Lavrent'ev,Panov,Kudryavtsev

, p. 1132 - 1135 (2002)

The possibility of preparing from dialkyl dihydrogen 3,3′,4,4′- benzophenonetetracarboxylates and 4,4′-diaminodiphenylmethane or 4,4′-diaminodiphenyl ether H complexes of both amorphous and crystalline structures was elucidated. Methods were proposed for disordering the supramolecular structure of the H complexes, which is technologically essential for reducing the melt viscosity when preparing polyimide carbon-filled plastics and foamed composites.

STUDY OF THE STRUCTURE OF SOLUTIONS OF THE H-COMPLEXES OF DIESTERS OF TETRACARBOXYLIC ACIDS WITH DIAMINES BY THE LIGHT SCATTERING METHOD. 1. H-COMPLEX OF THE DIMETHYL ESTER OF BENZOPHENONETETRACARBOXYLIC ACID WITH HEXAMETHYLENEDIAMINE

Chupans, P. I.,Kallistov, O. V.,Artem'eva, V. N.,Silinskaya, I. G.,Mel'nikova, G. G.,et. al.

, p. 1180 - 1184 (2007/10/02)

Conclusions about structure formation in solutions of the H-complexes of benzophenonetetracarboxylic acid with hexamethylenediamine have been drawn from the angular dependence of the intensity of scattered polarized light.The calculated statistical structural parameters show that the H-complexes form dipentameric associations.At high concentrations of the complexes in aqueous-methanolic solution the supermolecular structure is disrupted, while in the pure alcohol the reverse process is observed.

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