14832-57-6 Usage
Uses
Used in Organic Synthesis:
1-(Naphthalen-2-yl)-1H-tetrazol-5-amine is used as a building block for the synthesis of various organic compounds. Its naphthalene ring structure and tetrazole amine functionality contribute to the structural diversity and reactivity of the synthesized products, making it a valuable component in organic chemistry.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1-(Naphthalen-2-yl)-1H-tetrazol-5-amine is used as a key component in the development of new drugs. Its unique chemical properties allow it to be incorporated into drug candidates, potentially enhancing their efficacy and selectivity.
Used in Antimicrobial Applications:
1-(Naphthalen-2-yl)-1H-tetrazol-5-amine has been studied for its potential antimicrobial properties. It may be used as an active ingredient in the development of new antimicrobial agents, targeting a range of bacterial and fungal pathogens.
Used in Anticancer Applications:
1-(naphthalen-2-yl)-1H-tetrazol-5-amine has also been investigated for its potential anticancer properties. 1-(Naphthalen-2-yl)-1H-tetrazol-5-amine may be employed as an anticancer agent, contributing to the development of novel therapeutic strategies against various types of cancer.
Used in Medicinal Chemistry Research:
As a compound with potential medicinal applications, 1-(Naphthalen-2-yl)-1H-tetrazol-5-amine is an important subject of study in medicinal chemistry research. Its unique structure and properties make it a promising candidate for further exploration and development in the field of drug discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 14832-57-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,8,3 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 14832-57:
(7*1)+(6*4)+(5*8)+(4*3)+(3*2)+(2*5)+(1*7)=106
106 % 10 = 6
So 14832-57-6 is a valid CAS Registry Number.
14832-57-6Relevant articles and documents
Magnetic chitosan-copper nanocomposite: A plant assembled catalyst for the synthesis of amino- and N-sulfonyl tetrazoles in eco-friendly media
Motahharifar, Narjes,Nasrollahzadeh, Mahmoud,Taheri-Kafrani, Asghar,Varma, Rajender S.,Shokouhimehr, Mohammadreza
, (2020/01/08)
A greener, cost efficient and simple method is described to prepare copper nanoparticles (NPs) immobilized on the magnetic chitosan (one of the more versatile polysaccharides) using Euphorbia falcata leaf extract as reducing/stabilizing agent. The prepare
On the Physicochemical Characterization of 5-Amino-1-aryl-1H-tetrazoles: Electronic Molecule Parameters from the Thermal Isomerization into 5-Arylamino-1H-tetrazoles
Schelenz, Thomas,Schaefer, Wieland
, p. 197 - 200 (2007/10/03)
The known thermal isomerization of 5-amino-1-aryl-1H-tetrazoles (A) into corresponding 5-arylamino-1H-tetrazoles (HB) was used to derive physicochemical parameters characterizing the electronic substituent effect on isomerism and dissociation equilibria. For a series of 26 tetrazoles A as starting materials the equilibrium constants (pKi) of isomerization in boiling ethylene glycol at 197°C and the dissociation constants (pKa) of the NH-acidic tetrazoles HB were determined by potentiometric titration of rapidly cooled equilibrium mixtures in water and ethanol/water with KOH at 25°C. The pK values are closely correlated with Hammett's electronic substituent constants σ and can be used as electronic molecule parameters in QSAR or QSPR (QSAR = quantitative structure-activity relationship; QSPR = quantitative structure-property relationship) studies.
