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1,2,5,6-Tetraphenyltricyclo[4.2.0.0^2,5^]octane is a complex organic compound characterized by its unique tricyclic structure. It consists of three fused rings, with the central ring being a cyclooctane, which is an eight-carbon ring. The compound is adorned with four phenyl groups (C6H5-), which are benzene rings, attached to the carbon atoms at positions 1, 2, 5, and 6 of the tricycle. This arrangement of phenyl groups significantly influences the compound's physical and chemical properties, such as its stability, reactivity, and potential applications in areas like materials science and organic chemistry. The compound's structure also suggests that it may exhibit interesting stereochemistry and could be a subject of study in the synthesis of complex organic molecules.

4759-04-0

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4759-04-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4759-04-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,5 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4759-04:
(6*4)+(5*7)+(4*5)+(3*9)+(2*0)+(1*4)=110
110 % 10 = 0
So 4759-04-0 is a valid CAS Registry Number.

4759-04-0Relevant 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

Photochemical Reactions of Model cis-Stilbenes: The -Cycloaddition Reaction

Penn, John H.,Gan, Li-Xian,Eaton, Thomas A.,Chan, Edward Y.,Lin, Zhe

, p. 1519 - 1523 (2007/10/02)

The photochemical -reactions of three model cis-stilbenes have been examined. 1,2-Diphenylcyclobutene was found to undergo photochemical -cycloaddition reactions with 2,5-dimethyl-2,4-hexadiene and with itself but did not undergo reaction with tetramethylethylene. 1,2-Diphenylcyclopentene and 1,2-diphenylcyclohexene were unreactive in photochemical -cycloaddition reactions.The singlet excited-state lifetimes of these compounds were measured.The results show that the observation of the cis-stilbene -reaction is dependent upon the rate of deactivation of the excited state.

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