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1,2,3,4-Tetrahydronaphthalen-1-one (2,4-dinitrophenyl)hydrazone is a complex organic compound with the molecular formula C16H14N4O4. It is derived from the parent compound tetrahydronaphthalen-1-one, which is a saturated derivative of naphthalene, a bicyclic aromatic hydrocarbon. The compound is characterized by the presence of a hydrazone functional group, formed by the reaction of the carbonyl group of the tetrahydronaphthalen-1-one with the 2,4-dinitrophenylhydrazine. The 2,4-dinitrophenyl group is an electron-withdrawing substituent, which can significantly influence the chemical reactivity and physical properties of the molecule. 1,2,3,4-tetrahydronaphthalen-1-one (2,4-dinitrophenyl)hydrazone may be of interest in organic chemistry research, particularly in the study of hydrazone derivatives and their potential applications in various fields, such as pharmaceuticals or materials science.

853-95-2

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853-95-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 853-95-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,5 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 853-95:
(5*8)+(4*5)+(3*3)+(2*9)+(1*5)=92
92 % 10 = 2
So 853-95-2 is a valid CAS Registry Number.

853-95-2Relevant academic research and scientific papers

Fe (III) complexes of a bis-benzimidazolyl diamide ligand: Spectral and Catalytic studies

Ahuja, Gauri,Mathur, Pavan

, p. 180 - 186 (2011)

A new tetradentate bis benzimidaozlyl diamide ligand N,N′-Bis (benzimidazol-2-yl-methyl)-hexane-1,6-dicarboxamide (GBSA) has been synthesized and utilized to prepare new Fe(III) complexes with exogenous anionic ligand X = Cl- and NO3-. Isomer shift values are in the range found for Iron in the +3 oxidation state while Quadrupole Splitting indicates large distortion from a six coordinate geometry, a finding supported by low temperature EPR work. The E1/2 values are found to be quite cathodic indicating stability of the Iron (III) complexes. The oxidation of alcohols was investigated using [Fe(GBSA)Cl3] as the catalyst with TBHP as an alternate source of oxygen. The respective carbonyl products have been isolated and characterized by 1H NMR, electronic spectroscopy, mass and IR spectral studies.

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