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136296-63-4

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136296-63-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136296-63-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,2,9 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 136296-63:
(8*1)+(7*3)+(6*6)+(5*2)+(4*9)+(3*6)+(2*6)+(1*3)=144
144 % 10 = 4
So 136296-63-4 is a valid CAS Registry Number.

136296-63-4Downstream Products

136296-63-4Relevant articles and documents

Tuning J-aggregate Formation and Emission Efficiency in Cationic Diazapentacenium Dyes

Rodrigues, Ana Clara B.,Wetterling, Dario,Scherf, Ullrich,Seixas de Melo, J. Sérgio

, p. 7826 - 7830 (2021)

Enhancement of the luminescence efficiency of two new diazapentacenium salts (D1 and D2) of more than 55 for D1 and 22 times for D2) in poor solvents, acetonitrile and/or dichloromethane, was observed and rationalized as formation of emissive J-aggregates. Both compounds displaying 4-n-decylphenyl substituents at the 7,14-carbons and phenyl (D1) or 2,6-difluorophenyl (D2) substituents at the quaternary nitrogen atoms in 5,12-positions have been synthetized in a two-step procedure involving a two-fold Buchwald-Hartwig-type CN cross-coupling and an electrophilic Friedel-Crafts-type cyclization. The optical properties of the dicationic diazapentacenium salts in various solvents and in thin films have been investigated by steady-state and time-resolved absorption and photoluminescence spectroscopies. In thin films and in good solvents, isolated molecules coexist with aggregates. Nonetheless, D1 is seven times more emissive than D2, reflecting a higher J-aggregate contribution in the former.

Synthesis and properties of an acetal-bridged ladder poly(p-phenylene)

Lee, Myunggun,Hahn, So-Jung,Poduval, Mithrabinda K.K.,Kim, Tae-Hyun

scheme or table, p. 2776 - 2778 (2012/02/01)

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