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Anthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline-1,3,8,10(2H,9H)-tetrone, 2,9-dicyclohexyl-5,12-bis(1,2,2-triphenylethenyl)- is a complex organic compound characterized by its unique molecular structure. It features a central anthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline core, which is a fused ring system with alternating single and double bonds. The compound is further defined by the presence of a tetrone group, indicating four carbonyl (C=O) groups, and a 2,9-dicyclohexyl substitution, which means two cyclohexyl groups are attached to the 2nd and 9th carbon atoms of the core structure. Additionally, it has two 1,2,2-triphenylethenyl groups attached to the 5th and 12th positions, which are phenyl-substituted ethylene moieties. Anthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline-1,3,8,10(2H,9H)-tetrone, 2,9-dicyclohexyl-5,12-bis(1,2,2-triphenylethenyl)- is likely to be of interest in the field of organic chemistry, potentially for its electronic properties or as a precursor in the synthesis of more complex molecules.

1365542-76-2

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1365542-76-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1365542-76-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,5,5,4 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1365542-76:
(9*1)+(8*3)+(7*6)+(6*5)+(5*5)+(4*4)+(3*2)+(2*7)+(1*6)=172
172 % 10 = 2
So 1365542-76-2 is a valid CAS Registry Number.

1365542-76-2Downstream Products

1365542-76-2Relevant academic research and scientific papers

Tetraphenylethenyl-modified perylene bisimide: Aggregation-induced red emission, electrochemical properties and ordered microstructures

Zhao, Qiuli,Zhang, Shuang,Liu, Yi,Mei, Ju,Chen, Sijie,Lu, Ping,Qin, Anjun,Ma, Yuguang,Sun, Jing Zhi,Tang, Ben Zhong

, p. 7387 - 7394 (2012)

Perylene bisimides (PBIs) are one class of the most explored organic fluorescent materials due to their high fluorescence quantum efficiency, electron transport behaviour, and ready to form well-tailored supramolecular structures. However, they suffer from heavy aggregation-caused quenching (ACQ) effect which has greatly limited their potential applications. We successfully tackle this problem by chemical modification of the PBI core with two tetraphenylethene (TPE) moieties at the bay positions. This modification resulted in a pronounced fluorescence red-shift (over 120 nm) and rendered the derivatives (1,6-/1,7-DTPEPBI) with evident aggregation-induced emission (AIE) behaviour. Both 1,6-DTPEPBI and 1,7-DTPEPBI emit bright red fluorescence in the solid state. The fluorescence quantum efficiency of the aggregates of 1,7-DTPEPBI (ΦF, solid = 29.7%, formed in a hexane/ dichloromethane mixture, fh = 90%) is about 424 times higher than that in dichloromethane solution (ΦF, solut = 0.07%). Electrochemical investigation results indicated that 1,7-DTPEPBI sustained the intrinsic n-type semiconductivity of PBI moiety. In addition, morphological inspection demonstrated that 1,7-DTPEPBI molecules easily form well-organized microstructures despite the linkage of the PBI core with bulky TPE moieties.

PHOTOTHERMAL AGENTS

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Page/Page column 33, (2020/02/14)

A photothermal agent can be used in both photoacoustic imaging (PAI) and photothermal therapy (PTT) applications. The photothermal agent can include a small molecule, organic compound and/or polymers with absorption in the near-infrared (NIR) interrogatio

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