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(1R,2S,2aS,10bR)-1,2-Bis-(4-methoxy-phenyl)-1,10b-dihydro-2H-cyclobuta[l]phenanthrene-2a-carbonitrile is a complex organic compound with a molecular formula of C27H23NO2. It features a cyclobuta[l]phenanthrene core, which is a type of polycyclic aromatic hydrocarbon. The molecule has two 4-methoxy-phenyl groups attached at the 1 and 2 positions, contributing to its overall structure and properties. The presence of a carbonitrile group at the 2a position further characterizes (1R,2S,2aS,10bR)-1,2-Bis-(4-methoxy-phenyl)-1,10b-dihydro-2H-cyclobuta[l]phenanthrene-2a-carbonitrile. This specific arrangement of atoms and functional groups gives the molecule unique chemical and physical properties, making it potentially useful in various applications, such as in pharmaceuticals or materials science, where its specific stereochemistry and functional groups could play a role.

79606-65-8

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79606-65-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79606-65-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,6,0 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 79606-65:
(7*7)+(6*9)+(5*6)+(4*0)+(3*6)+(2*6)+(1*5)=168
168 % 10 = 8
So 79606-65-8 is a valid CAS Registry Number.

79606-65-8Downstream Products

79606-65-8Relevant academic research and scientific papers

Photochemistry of the Phenanthrene-Stilbene System. Cycloaddition and Singlet-Sensitized Isomerization

Caldwell, Richard A.,Mizuno, Kazuhiko,Hansen, P. E.,Vo, L. P.,Frentrup, M.,Ho, C. D.

, p. 7263 - 7269 (1981)

Photocycloaddition of phenanthrenes to stilbenes is a general and remarkably facile reaction.Two isomeric trans adducts often result with unsymmetrical phenanthrenes.The product with cis-stilbene and 9-cyanophenanthrene is the crowded cis,endo isomer.With 9-cyanophenanthrene and trans-stilbene, geometric isomerization occurs but only in a triplet process.With cis-stilbene, geometric isomerization results from the triplet, and both geometric and valence isomerizations can be induced by singlet 9-cyanophenanthrene.The reactivity of the stilbene isomers can be accounted for by an algorithm we have previously derived, as can the 20- to 30-fold enhancement of stylbenes over styrenes as a reactant in cycloaddition to phenanthrene.The possibility of singlet-sensitized valence isomerization as a mechanism for storage of solar energy is discussed.

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