129-44-2 Usage
Description
1,5-Diaminoanthraquinone (DAAQ) is an organic dye compound known for its unique properties and potential applications in various fields. It has been studied for its absorption and fluorescence spectra in different organic solvents and has demonstrated the ability to form nanofibers (DAAQNFs) decorated with small platinum nanoparticles (PtNPs).
Uses
Used in Chemical Synthesis:
1,5-Diaminoanthraquinone is used as a precursor in the synthesis of poly(1,5-diaminoanthraquinone) (PDAA) particles through chemically oxidative polymerization. This process allows for the creation of novel materials with potential applications in various industries.
Used in Material Science:
1,5-Diaminoanthraquinone is used as a component in the preparation of vertical nanowire arrays. These arrays can be created using a facile physical vapor transport method, which may have significant implications for the development of advanced materials and devices in the fields of electronics, optoelectronics, and energy storage.
Used in Nanotechnology:
The rapid preparation of 1,5-diaminoanthraquinone nanofibers (DAAQNFs) decorated with small platinum nanoparticles (PtNPs) has been reported. This application highlights the potential of DAAQ in nanotechnology, where it can be utilized to create novel nanostructures with enhanced properties and functionalities.
Purification Methods
Recrystallise it from aniline (m 313-314o) EtOH or acetic acid [Flom & Barbara J Phys Chem 89 4481 1985]. [Beilstein 14 H 303, 14 I 467, 14 II 116, 14 III 466, 14 IV 479.]
Check Digit Verification of cas no
The CAS Registry Mumber 129-44-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,2 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 129-44:
(5*1)+(4*2)+(3*9)+(2*4)+(1*4)=52
52 % 10 = 2
So 129-44-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H10N2O2/c15-9-5-1-3-7-11(9)14(18)8-4-2-6-10(16)12(8)13(7)17/h1-6H,15-16H2
129-44-2Relevant articles and documents
Vertical organic nanowire arrays: Controlled synthesis and chemical Sensors
Yong, Sheng Zhao,Jinsong, Wu,Jiaxing, Huang
, p. 3158 - 3159 (2009)
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A facile method for preparing substituted 1-aminoanthraquinones
Wormser,Sardessai,Abramson
, p. 3211 - 3222 (2007/10/02)
An efficient and simple preparation of α-substituted aminoanthraquinones using 2,2,-dialkoxyethylamines is described.
Ring Opening Reactions of 6H-Anthraisoxazol-6-ones and Related Compounds
Sutter, P.,Weis, C. D.
, p. 997 - 1011 (2007/10/02)
Nucleophilic attack of anthraisoxazol-6-ones, and of anthraisoxazole by various sulfoxides, triphenyl phosphine, and aliphatic or aromatic phosphites proceeded with cleavage of the nitrogen-oxygen bond of the isoxazole ring.This method provided ready access to substituted anthraquinones bearing sulfoximido-, triphenylphosphazo-, and dialkyl(aryl)phosphoramidic groups attached to the 1- and the 1,5-positions of the anthraquinone system.The structures of the newly synthesized anthraquinone derivatives were supported by analytical and spectral data. 1 -S,S-dimethyl-N-(5-benzamidoanthraquinon-1-yl)sulfoximide yielded in 90percent sulfuric acid the 1-amino-5-sulfoximido anthraquinone without hydrolyzing the sulfoximido group.