5386-23-2 Usage
Uses
Used in Organic Synthesis:
2-Hydroxynaphthalen-1-ylmethylamine is used as a building block in organic synthesis for its ability to form various molecular structures. Its reactivity allows for the creation of new compounds with potential applications in different fields.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-Hydroxynaphthalen-1-ylmethylamine is used as a precursor in the development of new drugs. Its unique structure and reactivity make it a valuable tool for studying the relationships between chemical structure and biological activity, potentially leading to the discovery of novel therapeutic agents.
Although 2-Hydroxynaphthalen-1-ylmethylamine does not have any significant industrial applications, its role in scientific research and development is crucial, as it contributes to the advancement of organic chemistry and pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 5386-23-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,8 and 6 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5386-23:
(6*5)+(5*3)+(4*8)+(3*6)+(2*2)+(1*3)=102
102 % 10 = 2
So 5386-23-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H11NO/c12-7-10-9-4-2-1-3-8(9)5-6-11(10)13/h1-6,13H,7,12H2
5386-23-2Relevant academic research and scientific papers
Voltammetric, potentiometric and spectrophotometric studies of some hydrazones and their metal complexes in ethanolic-aqueous buffered solutions
Ghoneim, Mohammed M.,El-Hallag, Ibrahim S.,El-Baradie, Kamal Y.,El-Desoky, Hanaa S.,El-Attar, Mona A.
, p. 285 - 299 (2007/10/03)
The electrochemical behavior of some hydrazones derived from 6-chloro-2-hydrazinopyridine in the Britton-Robinson universal buffer of pH 2-11 containing 35% ethanol was investigated at the mercury electrode using dc-polarography, controlled-potential coulometry, and cyclic voltammetry techniques. The examined hydrazones were reduced in solutions of pH 2 single bond. The mechanistic pathway of the electrode reaction of the studied compounds was elucidated and discussed. The pK a values of the examined hydrazones and the stoichiometry of their complexes in solution with some transition metal ions were determined spectrophotometrically. The dissociation constants and the thermodynamic parameters of the investigated hydrazones, and the stability constants of their metal complexes in solution were determined potentiometrically. Springer-Verlag 2006.
