54582-22-8 Usage
Uses
Used in Organic Synthesis:
Ethanone, 1-(2-hydroxyphenyl)-, oxime, (E)is utilized as an intermediate in organic synthesis for the production of various organic compounds. Its unique structure allows for versatile reactions, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used as a Chelating Agent:
In the field of analytical chemistry, Ethanone, 1-(2-hydroxyphenyl)-, oxime, (E)serves as a chelating agent, capable of forming stable complexes with metal ions. This property is particularly useful in the detection and separation of metal ions in environmental and biological samples, as well as in the development of new analytical methods.
Used in Pharmaceutical Industry:
Ethanone, 1-(2-hydroxyphenyl)-, oxime, (E)is employed in the pharmaceutical industry for its potential therapeutic applications. Its unique structure and reactivity make it a promising candidate for the development of new drugs, particularly in the areas of central nervous system disorders, cardiovascular diseases, and other therapeutic areas where its chelating and reactive properties can be harnessed for medicinal purposes.
Used in Chemical Research:
In the realm of chemical research, Ethanone, 1-(2-hydroxyphenyl)-, oxime, (E)is utilized as a model compound to study the properties and reactivity of oxime compounds. Its well-defined structure and configuration provide valuable insights into the behavior of similar compounds, contributing to the advancement of organic chemistry and the development of new synthetic methodologies.
Check Digit Verification of cas no
The CAS Registry Mumber 54582-22-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,5,8 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 54582-22:
(7*5)+(6*4)+(5*5)+(4*8)+(3*2)+(2*2)+(1*2)=128
128 % 10 = 8
So 54582-22-8 is a valid CAS Registry Number.
54582-22-8Relevant academic research and scientific papers
A mild system for synthesis of aldoximes and ketoximes in the presence of N-hydroxyphthalimide in aqueous system
Jiang, Xiaoying,Xu, Xiaohe,Lin, Yuyan,Yan, Yiyan,Li, Pingping,Bai, Renren,Xie, Yuanyuan
supporting information, p. 5879 - 5885 (2018/09/06)
An efficient method for synthesis of oximes from aldehydes or ketones with N-hydroxyphthalimide or N-hydroxysuccinimide in water has been described. It is the first time to utilize NHPI as an oximation reagent to synthesize aldoximes and ketoximes from the corresponding organic carbonyl compounds without other reagents. The reaction tolerates various functional groups and affords the corresponding oximes in 76%–98% yields. The by-product phthalic acid can be recycled from the system. In addition, this method has been successfully applied to the synthesis of the precursor of some pharmacologically active amide molecules.
Muscarinic agonists
-
, (2008/06/13)
Compounds and methods are provided for the treatment of disease conditions in which modification of cholinergic, especially muscarinic m1, m4, or both m1 and m4, receptor activity has a beneficial effect. In the method, an effective amount of a compound is administered to a patient in need of such treatment.
Bimetallic Complexes of Nickel(II) with Tin(IV) Chloride and Tellurium(IV) Chloride
Aminabhavi, T. M.,Biradar, N. S.,Raythatha, R. H.,Patil, M. D.
, p. 250 - 252 (2007/10/02)
A few binuclear complexes of nickel(II) with tin(IV) chloride or tellurium(IV) chloride have been synthesized.The complexes are light-blue to green in color and are nonelectrolytes in DMF solution.Elemental analysis suggests a 1:1 stoichiometry.Magnetic m
