59862-56-5 Usage
Description
(E)-N-[1-(4-nitrophenyl)ethylidene]hydroxylamine, also known as NEHA-Nitronaphthylhydroxylamine, is a chemical compound that belongs to the class of hydroxylamines. It is characterized by its potential applications in various fields, including analytical chemistry and therapeutic treatments.
Uses
Used in Analytical Chemistry:
(E)-N-[1-(4-nitrophenyl)ethylidene]hydroxylamine is used as a reagent for the determination of various compounds, such as sugars, aldehydes, and ketones. It plays a crucial role in the accurate identification and quantification of these substances in different samples.
Used in Environmental Monitoring:
In the field of environmental science, (E)-N-[1-(4-nitrophenyl)ethylidene]hydroxylamine is used as a detection agent for nitrite in water samples. Its ability to identify and measure nitrite levels is essential for assessing water quality and ensuring public health safety.
Used in Pharmaceutical Research:
(E)-N-[1-(4-nitrophenyl)ethylidene]hydroxylamine has been investigated for its potential as a therapeutic agent, particularly in the treatment of neurodegenerative diseases. Its unique chemical properties make it a promising candidate for further research and development in this area.
Used in Organic Chemistry:
In the realm of organic chemistry, (E)-N-[1-(4-nitrophenyl)ethylidene]hydroxylamine is employed in the identification of certain organic compounds. Its reactivity and specificity contribute to the advancement of chemical analysis and synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 59862-56-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,8,6 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 59862-56:
(7*5)+(6*9)+(5*8)+(4*6)+(3*2)+(2*5)+(1*6)=175
175 % 10 = 5
So 59862-56-5 is a valid CAS Registry Number.
59862-56-5Relevant articles and documents
One-pot synthesis of 2-amino-3,4-dicyanopyridines from ketoximes and tetracyanoethylene via Cu(I)-catalyzed cyclization
Han, Ziwei,Lv, Jianguang,Zhang, Jianmin
supporting information, p. 2162 - 2168 (2019/02/25)
A novel approach to 2-amino-3,4-dicyanopyridines has been discovered from Cu(I)-catalyzed cyclizations of simple and easily available ketoximes and tetracyanoethylene (TCNE). The complexed radical mechanism involves cleavage of several O[sbnd]H/N[sbnd]O/C
Stereospecific synthesis of 1,5-disubstituted tetrazoles from ketoximes via a Beckmann rearrangement facilitated by diphenyl phosphorazidate
Ishihara, Kotaro,Shioiri, Takayuki,Matsugi, Masato
supporting information, p. 1295 - 1298 (2019/04/13)
A novel method for the stereospecific synthesis of 1,5-disubstituted tetrazoles from ketoximes via the Beckmann rearrangement was developed using diphenyl phosphorazidate (DPPA) as both the oxime activator and azide source. Various ketoximes were transformed into the corresponding 1,5-disubstituted tetrazoles with exclusive trans-group migration and no E-Z isomerization of the ketoxime. This method enables the preparation of 1,5-disubstituted tetrazoles without using toxic or explosive azidation reagents.
Evaluation of Substituted 1,2,3-Dithiazoles as Inhibitors of the Feline Immunodeficiency Virus (FIV) Nucleocapsid Protein via a Proposed Zinc Ejection Mechanism
Asquith, Christopher R. M.,Konstantinova, Lidia S.,Laitinen, Tuomo,Meli, Marina L.,Poso, Antti,Rakitin, Oleg A.,Hofmann-Lehmann, Regina,Hilton, Stephen T.
, p. 2119 - 2126 (2016/10/22)
A diverse library of 5-thieno-, 5-oxo-, and 5-imino-1,2,3-dithiazole derivatives was synthesized and evaluated for efficacy against the feline immunodeficiency virus (FIV) as a model for HIV in cells. Several diverse compounds from this series displayed n