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6,7:8,9-dibenzo-1,5-dicyano-trans-2,4-diphenylbicyclo<3.2.2>nona-6,8-diene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

109423-45-2

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109423-45-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109423-45-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,4,2 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 109423-45:
(8*1)+(7*0)+(6*9)+(5*4)+(4*2)+(3*3)+(2*4)+(1*5)=112
112 % 10 = 2
So 109423-45-2 is a valid CAS Registry Number.

109423-45-2Downstream Products

109423-45-2Relevant academic research and scientific papers

Photochemistry of 9,10-Dicyanoanthracene-1,2-Diarylcyclopropane Systems. Photocycloaddition and Photoisomerization

Mizuno, Kazuhiko,Ichinose, Nobuyuki,Otsuji, Yoshio

, p. 1855 - 1860 (2007/10/02)

The photochemical reactions of 9,10-dicyanoanthracene (DCA)-1,2-diarylcyclopropane (CP) systems have been investigated.In degassed acetonitrile solution, (4? + 2?) photocycloaddition between DCA and CP occurred to give cis- and trans-2,4-diaryl-1,5-dicyano-6,7:8,9-dibenzobicyclonona-6,8-dienes in a 3:1 ratio in good chemical yields although the quantum yields were not high (Φ = 0.002 - 0.04).This photocycloaddition did not occur in benzene.The DCA-sensitized photoisomerization of trans- and cis-1,2-bis(4-methoxyphenyl)cyclopropanes (1a and 2a) in acetonitrile efficiently occurred to afford a photostationary mixture containing 1a and 2a in a 95:5 ratio.The photoisomerization was remarkably accelerated by bubbling air, by adding metal salts such as Mg(ClO4)2 and LiBF4, and also by aromatic hydrocarbons such as phenanthrene and biphenyl.The quantum yield for the photoisomerization of 2a to 1a exceeded unity, indicating that this photoisomerization involved a chain process.The DCA-sensitized photoisomerisation of optically resolved (-)-1a afforded a racemic mixture of (+)-1a and (-)-1a.These photoreactions are initiated by a one-electron transfer from CP to the excited singlet of DCA.The photocycloaddition proceeds via radical ion pairs in solvent cage and the photoisomerization proceeds via solvent-separated radical cations of CP.

(2?+4?) PHOTOCYCLOADDITION OF 1,2-DIARYLCYCLOPROPANES TO 9,10-DICYANOANTHRACENE VIA GEMINATE RADICAL ION PAIR

Ichinose, Nobuyuki,Mizuno, Kazuhiko,Hiromoto, Ziro,Otsuji, Yoshio

, p. 5619 - 5620 (2007/10/02)

Irradiation of a degassed acetonitrile solution containing 9,10-dicyanoanthracene (DCA) and 1,2-diarylcyclopropanes gave (2?+4?) photocycloadducts in good yields.The geminate radical ion pairs betwen DCA and the cyclopropanes are involved as key intermediates in this photoreaction.

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