7385-99-1 Usage
Uses
Used in Organic Synthesis:
PYRIDINE-2-CARBOXALDEHYDE 2-QUINOLYLHYDRAZONE is used as a reagent in organic synthesis for its ability to participate in a variety of chemical reactions, facilitating the formation of new compounds and contributing to the advancement of organic chemistry.
Used in Analytical Chemistry:
In the field of analytical chemistry, PYRIDINE-2-CARBOXALDEHYDE 2-QUINOLYLHYDRAZONE is used for its fluorescence properties, which can be leveraged for the detection and analysis of various substances, enhancing the sensitivity and specificity of analytical methods.
Used in Biochemistry:
PYRIDINE-2-CARBOXALDEHYDE 2-QUINOLYLHYDRAZONE's fluorescence also makes it a valuable tool in biochemistry, where it can be used to study biological processes and interactions at the molecular level, potentially aiding in the development of new diagnostic and therapeutic approaches.
Used in Pharmaceutical Research:
PYRIDINE-2-CARBOXALDEHYDE 2-QUINOLYLHYDRAZONE is used as a subject of research in pharmaceutical applications due to its potential anti-inflammatory and anti-cancer properties. Further investigation is required to fully understand its therapeutic potential and to develop it into a viable pharmaceutical agent.
Used in Research and Development:
In the context of research and development, PYRIDINE-2-CARBOXALDEHYDE 2-QUINOLYLHYDRAZONE serves as a compound of interest for scientists exploring new chemical reactions, synthesis methods, and potential applications in various industries, including materials science and environmental chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 7385-99-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,8 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7385-99:
(6*7)+(5*3)+(4*8)+(3*5)+(2*9)+(1*9)=131
131 % 10 = 1
So 7385-99-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H12N4/c1-2-7-14-12(5-1)8-9-15(18-14)19-17-11-13-6-3-4-10-16-13/h1-11H,(H,18,19)/b17-11+
7385-99-1Relevant academic research and scientific papers
Synthesis and Characterization of 2-Pyridinylmethylene-2-quinolyl Hydrazone Cobalt(III) Complexes. Reactivity Trends and Solvent Effect on the Initial and Transition States of Base Catalyzed Hydrolysis
Mohamad, Ahmad Desoky M.
, p. 1575 - 1595 (2017/09/06)
The complexes of pyridine-2-aldehyde-2-quinolylhydrazone Co(III) nitrate [Co(paqh)2](NO3)2, methyl-2-pyridylketone-2-quinolinhyrazone Co(III) nitrate [Co(mpkqh)2](NO3)2, and phenyl-2-pyridylketon-2-quinolinhyrazone Co(III) nitrate [Co(ppkqh)2](NO3)2 were prepared and characterized. Solubilities of Co(III)–hydrazone complexes were measured. Transfer chemical potentials were calculated from the measured solubilities of the Co(III) complexes in aqueous methanol mixtures at 25?°C. The reactivity trends in the transfer chemical potentials are discussed in terms of the nature of the bonded ligands. Kinetics of the base hydrolysis of Co(III)–hydrazone complexes in the aqueous methanol mixtures have been studied at 25?°C, and follow the rate law kobs?=?k2[OH?]. The solvent effects on the reactivity trends of Co(III) complexes are analyzed into initial state (is) and transition states (ts) components. The reaction rates are reduced by the increase of methanol content. The destabilization of the transition state is remarkable compared to the initial state in the aqueous methanol mixtures. The initial state is more hydrophobic in nature than the transition state for Co(III) complex reactions.
Medicinal uses of hydrazones
-
, (2008/06/13)
Compounds having a structure according to Formula (I): are effective in a method of increasing erythropoietin and vascularization of tissue in a subject in need thereof.
