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1-Ethynyl-3,5,7-trimethyladamantane is a complex organic compound with the molecular formula C14H20. It is a derivative of adamantane, a highly stable and rigid hydrocarbon with a symmetrical structure resembling a diamond. The compound features a triple-bonded carbon chain (ethynyl group) at the 1-position, and three methyl groups attached to the 3, 5, and 7 carbon atoms. This structure endows the molecule with unique chemical and physical properties, making it a potential candidate for various applications in the fields of materials science, pharmaceuticals, and chemical research. Due to its stability and unique structure, 1-ethynyl-3,5,7-trimethyladamantane can be used in the synthesis of other complex organic molecules and as a building block for advanced materials with specific properties.

7167-32-0

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7167-32-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7167-32-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,6 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7167-32:
(6*7)+(5*1)+(4*6)+(3*7)+(2*3)+(1*2)=100
100 % 10 = 0
So 7167-32-0 is a valid CAS Registry Number.

7167-32-0Downstream Products

7167-32-0Relevant academic research and scientific papers

Arrays of Molecular Rotors with Triptycene Stoppers: Surface Inclusion in Hexagonal Tris(o -phenylenedioxy)cyclotriphosphazene

Kaleta, Ji?í,Dron, Paul I.,Zhao, Ke,Shen, Yongqiang,Císa?ová, Ivana,Rogers, Charles T.,Michl, Josef

, p. 6173 - 6192 (2015)

A new generation of rod-shaped dipolar molecular rotors designed for controlled insertion into channel arrays in the surface of hexagonal tris(o-phenylenedioxy)cyclotriphosphazene (TPP) has been designed and synthesized. Triptycene is used as a stopper intended to prevent complete insertion, forcing the formation of a surface inclusion. Two widely separated 13C NMR markers are present in the shaft for monitoring the degree of insertion. The structure of the two-dimensional rotor arrays contained in these surface inclusions was examined by solid-state NMR and X-ray powder diffraction. The NMR markers and the triptycene stopper functioned as designed, but half of the guest molecules were not inserted as deeply into the TPP channels as the other half. As a result, the dipolar rotators were distributed equally in two planes parallel to the crystal surface instead of being located in a single plane as would be required for ferroelectricity. Dielectric spectroscopy revealed rotational barriers of ~4 kcal/mol but no ferroelectric behavior.

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