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341556-86-3

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341556-86-3 Usage

Description

(2E,2’E)-3,3’-(anthracene-9,10-diyl)diacrylic acid is a fluorescent chemical compound characterized by two anthracene rings linked by a diacrylic acid bridge. This structure endows the compound with distinctive photophysical properties, making it a valuable tool for investigating energy transfer, molecular interactions, and other processes in biology and materials science. The presence of the diacrylic acid group also facilitates its integration into polymers and various materials, enhancing its utility in materials science and nanotechnology applications.

Uses

Used in Research and Development:
(2E,2’E)-3,3’-(anthracene-9,10-diyl)diacrylic acid serves as a fluorescent probe in biological and materials science research, enabling the study of energy transfer and molecular interactions due to its unique photophysical characteristics.
Used in Materials Science:
In the field of materials science, (2E,2’E)-3,3’-(anthracene-9,10-diyl)diacrylic acid is utilized for its ability to be incorporated into polymers and other materials, contributing to the development of advanced materials with specific properties.
Used in Nanotechnology:
(2E,2’E)-3,3’-(anthracene-9,10-diyl)diacrylic acid's fluorescent properties and compatibility with material integration make (2E,2’E)-3,3’-(anthracene-9,10-diyl)diacrylic acid a useful component in nanotechnology, where it can be employed in the design of nanoscale devices and systems with tailored functionalities.

Check Digit Verification of cas no

The CAS Registry Mumber 341556-86-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,1,5,5 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 341556-86:
(8*3)+(7*4)+(6*1)+(5*5)+(4*5)+(3*6)+(2*8)+(1*6)=143
143 % 10 = 3
So 341556-86-3 is a valid CAS Registry Number.

341556-86-3Downstream Products

341556-86-3Relevant articles and documents

Unprecedented Solvent-Dependent Sensitivities in Highly Efficient Detection of Metal Ions and Nitroaromatic Compounds by a Fluorescent Barium Metal-Organic Framework

Wang, Rongming,Liu, Xiaobin,Huang, Ao,Wang, Wen,Xiao, Zhenyu,Zhang, Liangliang,Dai, Fangna,Sun, Daofeng

, p. 1782 - 1787 (2016)

The assembly of a fluorescent dicarboxylate ligand with a barium ion resulted in the formation of a 3D metal-organic framework, Ba5(ADDA)5(EtOH)2(H2O)3·5DMF (UPC-17), based on a 1D rod-shaped secondary building unit. The unprecedented solvent-dependent sensitivities of UPC-17 for the detection of Fe3+/Al3+ ions and 4-nitrophenol with high efficiency were observed for the first time. Significantly, UPC-17 exhibits superior "turn-off" detection for the Fe3+ ion in methanol and acetone emulsions but shows "turn-on" detection in tetrahydrofuran emulsion. Furthermore, the visible color changes in the detection process make them easy to distinguish by the naked eye, which further increases its application potential.

Acrylamide derivatives and process for production thereof

-

, (2008/06/13)

Acrylamide derivatives represented by General Formula (1) below: STR1 (One specific example of General Formula (1) is methyl (S,S)-3,3'-?3,3'-(1,4-phenylenediacryloyl)!-bis?1-chloromethyl-5-hydroxy-7-triflouromethyl-1, 2,3,6-tetrahydropyrrolo?3,2-e!indole-8-carboxylate.) The acrylamide derivatives represented by General Formula (1) is highly selective to cancer cells, less toxic, and highly active also against solid tumor.

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