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(+/-)-5,12-diphenyl-trans-5,5a,6,7,8,9,10,11,11a,12-decahydro-5,12-epoxido-cycloocta[b]naphthalene is a complex organic compound with a molecular formula of C26H24O. It features a cycloocta[b]naphthalene core, which is a type of polycyclic aromatic hydrocarbon, with a trans-decalin ring structure and an epoxide group at the 5,12 positions. The molecule also contains two phenyl groups attached at the 5 and 12 positions, which contribute to its overall structure and properties. (+/-)-5,12-diphenyl-trans-5,5a,6,7,8,9,10,11,11a,12-decahydro-5,12-epoxido-cycloocta[b]naphthalene is characterized by its unique arrangement of carbon and hydrogen atoms, as well as the presence of the epoxide group, which can participate in various chemical reactions. It is important to note that the compound is a mixture of two enantiomers, indicated by the (+/-) notation, which means it has both a right-handed and left-handed version.

2081-76-7

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2081-76-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2081-76-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,8 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2081-76:
(6*2)+(5*0)+(4*8)+(3*1)+(2*7)+(1*6)=67
67 % 10 = 7
So 2081-76-7 is a valid CAS Registry Number.

2081-76-7Relevant academic research and scientific papers

Planar chiral dialkoxysilane: Introduction of inherent chirality and high reactivity in conventional achiral alkene

Tomooka, Katsuhiko,Miyasaka, Shouji,Motomura, Shougo,Igawa, Kazunobu

supporting information, p. 7598 - 7602 (2014/07/07)

A simple eight-membered dialkoxysilane (E)-1 prepared from 2-pentene-1,5-diol, showed remarkably stable planar chirality along with high reactivity toward epoxidation, Diels-Alder reaction, and cycloaddition reaction with azide. Enriching alkenes: A simple eight-membered dialkoxysilane, prepared from 2-pentene-1,5-diol, shows remarkably stable planar chirality along with quite a high reactivity in epoxidation reactions, Diels-Alder reactions, and in cycloaddition reactions with azide (see scheme).

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