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3-N-[N’-(4-methylphenyl)acetamidino]benzanthrone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1415583-92-4

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1415583-92-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1415583-92-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,5,5,8 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1415583-92:
(9*1)+(8*4)+(7*1)+(6*5)+(5*5)+(4*8)+(3*3)+(2*9)+(1*2)=164
164 % 10 = 4
So 1415583-92-4 is a valid CAS Registry Number.

1415583-92-4Downstream Products

1415583-92-4Relevant academic research and scientific papers

Fluorescent substituted amidines of benzanthrone: Synthesis, spectroscopy and quantum chemical calculations

Gonta, Svetlana,Utinans, Maris,Kirilov, Georgii,Belyakov, Sergey,Ivanova, Irena,Fleisher, Mendel,Savenkov, Valerij,Kirilova, Elena

, p. 325 - 334 (2013/02/23)

Several new substituted amidine derivatives of benzanthrone were synthesized by a condensation reaction from 3-aminobenzo[de]anthracen-7-one and appropriate aromatic and aliphatic amides. The obtained derivatives have a bright yellow or orange fluorescence in organic solvents and in solid state. The novel benzanthrone derivatives were characterized by TLC analysis, 1H NMR, IR, MS, UV/vis, and fluorescence spectroscopy. The solvent effect on photophysical behaviors of these dyes was investigated, and the results showed that the Stoke's shift increased, whereas quantum yield decreased with the growth of the solvent polarity. The structure of some dyes was confirmed by the X-ray single crystal structure analysis. AM1, ZINDO/S and ab initio calculations using Gaussian software were carried out to estimate the electron system of structures. The calculations show planar configurations for the aromatic core of these compounds and two possible orientations of amidine substituents. The calculation results correlate well with red-shifted absorption and emission spectra of compounds.

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