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"Endo-cis-anti-cis-endo-1,2,3,4,4a,5,6,7,8,8a,9a,10a-dodecahydro-1,4:5,8-dimethanoanthracene-9,10-dione" is a complex organic compound with a unique molecular structure. It belongs to the class of anthracene derivatives, which are known for their aromatic properties and potential applications in various fields, such as pharmaceuticals and materials science. This specific compound features a dodecahedral carbon skeleton with multiple hydrogen atoms and two carbonyl groups at the 9 and 10 positions. The stereochemistry of the molecule is characterized by a series of cis and trans configurations, which influence its physical and chemical properties. The compound's name reflects its intricate structure, indicating the arrangement of atoms and bonds within the molecule. Despite its complexity, endo-cis-anti-cis-endo-1,2,3,4,4a,5,6,7,8,8a,9a,10a-Dodecahydro-1,4:5,8-dimethanoanthracene-9,10-dione represents an interesting area of study for chemists due to its potential applications and the challenges it poses in synthesis and characterization.

2065-48-7

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2065-48-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2065-48-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,6 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2065-48:
(6*2)+(5*0)+(4*6)+(3*5)+(2*4)+(1*8)=67
67 % 10 = 7
So 2065-48-7 is a valid CAS Registry Number.

2065-48-7Relevant academic research and scientific papers

The 1:1 and 2:1 adducts of cyclopentadiene with p-benzoquinone

Yates, Peter,Switlak, Krzysztof

, p. 1894 - 1900 (2007/10/02)

The exo-cis isomer (8) of the well-known endo-cis 1:1 adduct (4) of cyclopentadiene and p-benzoquinone has been obtained by heating the endo-cis-anti-cis-endo 2:1 adduct (13) with p-benzoquinone and also by haeting 4 alone.The exo-cis isomer of the 1:1 adduct (11) of cyclopentadiene and p-toluquinone has also been obtained for the first time.Heating of the 2:1 adduct 13 gives a mixture containing the endo-anti-exo isomer 15, the exo-anti-exo isomer 16, and 13.The structures of these two new isomers are assigned on the basis of (i) spectroscopic comparison with 13 and the known endo-syn-endo and endo-syn-exo isomers, 12 and 14; (ii) spectroscopic comparison of the corresponding tetrahydro compounds; and (iii) the conversion of tetrahydro 15 by oxidation and acetylation to the syn-hydroquinone diacetate 28, which is stereoisomeric with the anti-hydroquinone diacetate 25, prepared by similar treatment of tetrahydro 13,14, and 16.It is proposed that interconversion of the 1:1 adducts occurs via dissociation-recombination, interconversion of the tetrahydro 2:1 adducts occurs via enolization, while interconversion of the 2:1 adducts themselves can occur by both routes.

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