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1,4-bis((4-aminophenyl)amino)anthrancene-9,10-dione is a complex organic compound with the molecular formula C26H18N4O2. It is characterized by its anthracene core, which is a tricyclic aromatic hydrocarbon, and two aminophenyl groups attached to the 1 and 4 positions. These groups are further connected to the anthracene through amide linkages, and the compound also features two carbonyl groups at the 9 and 10 positions. This chemical is known for its potential applications in the field of materials science, particularly in the development of dyes and pigments, as well as in the study of photophysical properties due to its extended conjugated system. The compound's structure allows for significant electronic delocalization, which can influence its optical and electronic properties, making it a subject of interest for researchers in organic chemistry and materials science.

2944-29-8

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2944-29-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2944-29-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,4 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2944-29:
(6*2)+(5*9)+(4*4)+(3*4)+(2*2)+(1*9)=98
98 % 10 = 8
So 2944-29-8 is a valid CAS Registry Number.

2944-29-8Downstream Products

2944-29-8Relevant academic research and scientific papers

A new kind of H-acid monoazo-anthraquinone reactive dyes with surprising colour

Shan, Bin,Tong, Xing,Xiong, Wei,Qiu, Wenzhu,Tang, Bingtao,Lu, Rongwen,Ma, Wei,Luo, Yi,Zhang, Shufen

, p. 44 - 54 (2015/09/01)

A new kind of reactive dyes containing both monoazo and anthraquinone chromophores was obtained by using 1,4-bis((4-aminophenyl)amino)anthrancene- 9,10-dione as diazo component and 1-amino-8-naphthol-3,6-disulfonicacid (H-acid) derivatives as coupling components. The dyes were characterized by UV-Vis, IR, MS, 1H NMR and 13C NMR. The results showed that the maximum absorption wavelengths of the dyes were all about 590 nm, which indicated that they were a kind of blue dyes. 1H NMR and 13C NMR results revealed that there were two kinds of tautomerisms in dye structure and a new conjugated system formed between the anthraquinone ring and the phenyl azo linkage. Density functional theory (DFT) calculations also proved the formation of the new larger conjugated system from which the blue colour was generated. The fixations of the dyes on cotton were over 88% and the light fastness reached 5 grade.

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