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Triphenylene-2,3,6,7,10,11-hexacarboxylic acid hexamethyl ester is a complex organic compound with the molecular formula C36H30O6. It is derived from triphenylene, a polycyclic aromatic hydrocarbon, by substituting six of its hydrogen atoms with carboxyl groups and subsequently esterifying these carboxyl groups with methanol to form methyl esters. Triphenylene-2,3,6,7,10,11-hexacarboxylic acid hexamethyl ester is characterized by its hexagonal structure with six ester groups attached to the periphery. It is known for its potential applications in the synthesis of advanced materials, such as polymers and dendrimers, due to its unique structure and properties. The compound's stability and reactivity can be influenced by the electronic and steric effects of the ester groups, making it a subject of interest in organic chemistry and materials science.

66628-60-2

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66628-60-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66628-60-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,6,2 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 66628-60:
(7*6)+(6*6)+(5*6)+(4*2)+(3*8)+(2*6)+(1*0)=152
152 % 10 = 2
So 66628-60-2 is a valid CAS Registry Number.

66628-60-2Downstream Products

66628-60-2Relevant academic research and scientific papers

Hexaradialenes by successive ring openings of tris(alkoxytricyclobutabenzenes): Synthesis and characterization

Shinozaki, Shinya,Hamura, Toshiyuki,Ibusuki, Yousuke,Fujii, Kotaro,Uekusa, Hidehiro,Suzuki, Keisuke

supporting information; scheme or table, p. 3026 - 3029 (2010/07/05)

(Figure Presented) You rang m'lord? Thermally induced successive ring openings of tris (alkoxytricyclobutabenzene) to hexaradialene are described. The isomerization reaction was highly stereoselective to afford a stereodefined hexaradialene 1, given that the hydroxy groups on the four-membered rings were protected by bulky substituents.

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