17189-85-4 Usage
Chemical structure
A hydrazone derivative of naphthalen-2(1H)-one, formed by the condensation of 2-(2,4-dinitrophenyl)hydrazine with naphthalen-2(1H)-one.
Functional groups
Contains a hydrazone group, a naphthalene ring, and a 2,4-dinitrophenyl group.
Organic synthesis
Used as an intermediate in the synthesis of various organic compounds.
Medicinal chemistry
Potentially used in the development of new drugs.
Analytical chemistry
Utilized in the detection and quantification of various analytes due to the presence of the dinitrophenyl group.
Stability
Likely stable under normal laboratory conditions.
Reactivity
May react with reducing agents, nucleophiles, and electrophiles due to the presence of the hydrazone and nitro groups.
Appearance
Likely a solid, possibly with a yellow or orange color due to the presence of the dinitrophenyl group.
Solubility
Soluble in organic solvents such as ethanol, methanol, and dimethyl sulfoxide (DMSO).
Handling
Should be handled with care due to the presence of the nitro group, which can be explosive under certain conditions.
Disposal
Dispose of according to local regulations and guidelines for hazardous chemicals.
Synthesis
The compound is synthesized by the condensation of 2-(2,4-dinitrophenyl)hydrazine with naphthalen-2(1H)-one, resulting in the formation of a hydrazone compound.
Structural analysis
The compound can be characterized using techniques such as nuclear magnetic resonance (NMR) spectroscopy, infrared (IR) spectroscopy, and mass spectrometry (MS) to confirm its structure and purity.
Check Digit Verification of cas no
The CAS Registry Mumber 17189-85-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,8 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 17189-85:
(7*1)+(6*7)+(5*1)+(4*8)+(3*9)+(2*8)+(1*5)=134
134 % 10 = 4
So 17189-85-4 is a valid CAS Registry Number.
17189-85-4Relevant academic research and scientific papers
Chen, Jie,Lin, Qi,Li, Qiao,Li, Wen-Ting,Zhang, You-Ming,Wei, Tai-Bao
, p. 86627 - 86631 (2016)
We synthesized a new iodide ion (I-) chemosensor (CS) based on a hydrazone derivative obtained from the condensation of 2-hydroxy-1-naphthaldehyde and 2,4-dinitrophenylhydrazine. The CS showed selective colorimetric recognition of I-
Synthesis, binding ability, and cell cytotoxicity of fluorescent probes for l-arginine detection based on naphthalene derivatives: Experiment and theory
Li, Jie,Zhang, Yang,Chen, Yanmei,Shang, Xuefang,Ti, Tongyu,Chen, Hongli,Wang, Tianyun,Zhang, Jinlian,Xu, Xiufang
, (2017/09/06)
Inspired by biological related parts, Schiff base derivatives and functional groups of chemical modification can provide efficient detection method of amino acids. Therefore, we have designed and prepared 4 compounds based on Schiff base derivatives invol
Orthometallation in bidentate Schiff base ligands via C-H activation: Synthesis of ruthenium(III) organometallic complexes
Ghosh, Kaushik,Kumar, Rajan,Kumar, Sushil,Bala, Manju,Singh, Udai P.
, p. 831 - 837 (2015/10/28)
Schiff bases obtained by the reactions of substituted aromatic aldehydes with phenyl hydrazine or 2,4-dinitrophenyl hydrazine were synthesized and characterized by spectroscopic methods. Cyclometalated Ru(III) complexes of general formula, namely [Ru(L)(PPh3)2Cl], were synthesized from the Schiff bases via C-H bond activation and characterized by spectroscopic and electrochemical studies. In addition, one molecular structure of one of the complexes was determined by X-ray crystallography. The redox behavior of the complexes was examined by electrochemical studies, and one mechanism of orthometallation was investigated.
