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Benzoic acid, 4-(3,4-dicyanophenoxy)-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

355809-09-5

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355809-09-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 355809-09-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,5,8,0 and 9 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 355809-09:
(8*3)+(7*5)+(6*5)+(5*8)+(4*0)+(3*9)+(2*0)+(1*9)=165
165 % 10 = 5
So 355809-09-5 is a valid CAS Registry Number.

355809-09-5Downstream Products

355809-09-5Relevant academic research and scientific papers

Synthesis and biological evaluation of peptide-conjugated phthalocyanine photosensitizers with highly hydrophilic modifications

Li, Fu,Liu, Qian,Liang, Zhenzhen,Wang, Jin,Pang, Mingpei,Huang, Weiqiang,Wu, Wenjie,Hong, Zhangyong

, p. 3409 - 3422 (2016)

The selectivity of targeted photosensitizer delivery is a constant challenge for photodynamic therapy (PDT). Herein, with the aim of optimizing the affinity, selectivity and activity of peptide-conjugated photosensitizers for PDT therapy and fluorescence

Impact of peripheral groups on novel asymmetric phthalocyanine-based hole-transporting materials for perovskite solar cells

Guo, Junjie,Sun, Mengmeng,Meng, Xianfang,Zhu, Hongwei,Ma, Chao,Hu, Shiyan,Shen, Jiaqi,Wang, Qian,Gao, Jinghan

, (2020)

Three novel asymmetrical substituted phthalocyaninecobalt with nitro and (4-butyl formate) phenoxy, (4-propenyl-2-methoxy) phenoxy or (4-methyl formate) phenoxy as different bulky peripheral groups (CoPcNO2-OBFPh, CoPcNO2-OPMPh, CoPcNO2-OMFPh) are successfully developed and applied as dopant-free hole-transporting materials (HTMs) in perovskite solar cells (PSCs). The impact of the different peripheral groups on properties of these phthalocyanines is also investigated. For the modification of bulky aroxy peripheral groups, all of the three metallophthalocyanines exhibit good solubility, suitable hole mobility, high thermal stability, and appropriate HOMO and LUMO energy levels. The most effective device based on CoPcNO2-OBFPh demonstrates an impressive power conversion efficiency (PCE) of 13.91% under AM 1.5G standard conditions, while CoPcNO2-OPMPh and CoPcNO2-OMFPh devices exhibit relative lower PCE of 11.81% and 9.47% respectively. In addition, CoPcNO2-OBFPh-based PSC shows the best stability after 1008 h in air with 50% relative humidity at room temperature.

Synthesis and photophysical studies of asymmetric zinc phthalocyanine-magnetic nanoparticle conjugates

Gold Matlou, Gauta,Kobayashi, Nagao,Kimura, Mutsumi,Nyokong, Tebello

, p. 12309 - 12318 (2017)

This work reports on the synthesis and amide bond linkage of carboxylic acid functionalized asymmetric zinc phthalocyanine (ZnPc) complexes to amino magnetic nanoparticles (AMNPs). The work further compares the photophysical and photochemical parameters o

Enhancement of incident photon-to-current conversion efficiency for phthalocyanine-sensitized solar cells by 3D molecular structuralization

Mori, Shogo,Nagata, Morio,Nakahata, Yuki,Yasuta, Kazumasa,Goto, Ryota,Kimura, Mutsumi,Taya, Minoru

supporting information; experimental part, p. 4054 - 4055 (2010/05/01)

(Figure Presented) Enlarging the molecular size of zinc phthalocyanine (Pc) dyes three dimensionally with 2, 6-diphenylphenoxy substituents significantly reduced the aggregation of the dyes on a TiO2 surface. As a result, the incident photon-to-current conversion efficiency was improved not only in the Q band but over the whole absorption range, achieving 4.6% energy conversion efficiency under one-sun conditions. Electron lifetime measurements indicated that these Pc dyes do not enhance charge recombination, encouraging further development of Pc. Copyright

TETRAAZAPORPHYRIN-BASED COMPOUNDS AND THEIR USES

-

Page/Page column 30-31, (2008/06/13)

Asymmetrically substituted metal-phthalocyanine compounds are disclosed. These compounds and other phthalocyanine-derivatives are used in bioimaging, bioanalysis, FRET and quenching techniques, photodynamic therapy, DNA analysis for cells, proteins, tissues and other biological entities, and other applications. Near- infrared fluorescence minimizes matrix effects typically seen in other methods of analyzing biochemical entities in cells, proteins, tissues and other biological entities.

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