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Ethanone, 1-(4-butoxyphenyl)-, oxime, also known as 4-Butylphenyl methyl ketoxime, is a chemical compound belonging to the oxime class. It has a molecular formula of C14H21NO and is characterized by its ability to form strong and stable complexes with metal ions, making it a useful chelating agent. This property, along with its potential antioxidant properties and free radical scavenging ability, makes it a promising candidate for various applications in pharmaceuticals, agrochemicals, and industrial processes.

91563-69-8

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91563-69-8 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
Ethanone, 1-(4-butoxyphenyl)-, oxime is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique ability to form stable complexes with metal ions allows for the development of new compounds with enhanced properties and therapeutic effects.
Used in Industrial Applications:
As a chelating agent, Ethanone, 1-(4-butoxyphenyl)-, oxime is used in metal extraction and purification processes. Its strong affinity for metal ions enables efficient separation and recovery of valuable metals from various sources.
Used in Drug Development:
Ethanone, 1-(4-butoxyphenyl)-, oxime has been studied for its potential antioxidant properties and its ability to scavenge free radicals. This makes it a promising candidate for the development of new drugs with therapeutic applications, particularly in the treatment of oxidative stress-related diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 91563-69-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,5,6 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 91563-69:
(7*9)+(6*1)+(5*5)+(4*6)+(3*3)+(2*6)+(1*9)=148
148 % 10 = 8
So 91563-69-8 is a valid CAS Registry Number.

91563-69-8Relevant academic research and scientific papers

Structure-activity analysis of a class of orally active hydroxamic acid inhibitors of leukotriene biosynthesis

Summers,Gunn,Martin,Martin,Mazdiyasni,Stewart,Young,Bouska,Dyer,Brooks,Carter

, p. 1960 - 1964 (2007/10/02)

The nature of the carbonyl and nitrogen substituents of hydroxamic acids has a major influence on the biological profile of these compounds. Hydroxamates with small groups such as methyl appended to the carbonyl and relatively large nitrogen substituents

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