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1,2,5,6-Tetraphenyl-1,5-cyclooctadiene is a complex organic compound characterized by its unique structure, which consists of a cyclooctadiene ring with four phenyl groups attached to it. This molecule is known for its rigid and planar structure, which is a result of the conjugation between the phenyl rings and the cyclooctadiene moiety. It is often used in organic chemistry as a ligand in coordination complexes, particularly in the formation of metal complexes with transition metals. The compound's stability and electronic properties make it a valuable tool in the study of organometallic chemistry and catalysis. Its synthesis typically involves the reaction of cyclooctatetraene with benzene in the presence of a catalyst, such as aluminum chloride, to form the tetraphenyl-substituted cyclooctadiene. 1,2,5,6-tetraphenyl-1,5-cyclooctadiene is also of interest due to its potential applications in materials science and as a precursor in the synthesis of other complex organic molecules.

4662-93-5

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4662-93-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4662-93-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,6 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4662-93:
(6*4)+(5*6)+(4*6)+(3*2)+(2*9)+(1*3)=105
105 % 10 = 5
So 4662-93-5 is a valid CAS Registry Number.

4662-93-5Relevant academic research and scientific papers

Electron-Transfer-Induced Rearrangements of Phenylated Tricyclo2,5>octane and 1,5-Cyclooctadiene

Hasegawa, Eietsu,Mukai, Toshio,Yanagi, Kazunori

, p. 2053 - 2058 (2007/10/02)

The hitherto unknown examples of cation radical isomerizations of tricyclo2,5>octane and 1,5-cyclooctadiene derivatives are reported.Photoreaction of 1,2,5,6-tetraphenyltricyclo2,5>octane (1) with 9,10-dicyanoanthrace

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