14181-83-0

Usage

Uses

Used in Pharmaceutical Industry:
Ethanone, 2-bromo-1-(4-methoxyphenyl)-, oxime is used as a starting material for the synthesis of various biologically active compounds. Its unique structure and reactivity make it a valuable component in the development of new drugs.
Used in Organic Chemistry Research:
As a member of the oxime class of compounds, Ethanone, 2-bromo-1-(4-methoxyphenyl)-, oxime serves as a reagent in organic chemistry reactions, contributing to the advancement of chemical knowledge and the discovery of novel chemical processes.
Used in Agricultural Industry:
Ethanone, 2-bromo-1-(4-methoxyphenyl)-, oxime has the potential to be used as a crop protection agent, offering new possibilities for pest control and crop enhancement. However, its toxicity and environmental impact must be carefully evaluated to ensure safe and sustainable use in agriculture.

Upstream product

• 2632-13-5 2-Bromo-4'-methoxyacetophenone 
• 100-06-1 1-(4-methoxyphenyl)ethanone 

Downstream Products

• 100181-22-4 3-(4-Methoxy-phenyl)-6,6-diphenyl-4H-[1,5,2]oxathiazine 
• 100181-23-5 3-(4-Methoxy-phenyl)-6,6-di-p-tolyl-4H-[1,5,2]oxathiazine 
• 227082-11-3 4-(p-methoxyphenyl)-3-hydroxythiazole-2(3H)-thione 
• 1204410-53-6 C₆₉H₉NO₂ 
• 1313999-04-0 2-(2-aminophenylamino)-1-(4-methoxyphenyl)ethanone oxime 
• 1423156-44-8 C₁₁H₁₅NO₃ 
• 1423156-24-4 C₁₁H₁₅NO₃ 
• 2632-13-5 2-Bromo-4'-methoxyacetophenone 
• 152801-66-6 C₁₅H₂₂NO₆P 
• 152801-89-3 diethyl 2-amino-2-(4-methoxyphenyl)ethylphosphonate 
• 780815-74-9 C₁₁H₁₂BrNO₃ 

Relevant academic research and scientific papers

An efficient synthesis of 2-isoxazolines from α-haloketone oximes and dimethyl sulfonium salts

2-Isoxazolines were synthesized efficiently from a formal [4+1] cycloaddition of nitrosoalkenes and sulfur ylides, which were generated in situ from α-haloketone oximes and dimethyl sulfonium salts. This approach provides a new method to synthesize a rang

Sodium nitrite catalyzed aerobic oxidative deoximation under mild conditions

A mild, simple process for the effective deoximation of a wide range of ketoximes and aldoximes has been developed, which utilizes available NaNO 2 as the catalyst and molecular oxygen as the green oxidant. Notably Amberlyst-15, which acts as the initiator of NaNO2, can be reused without regeneration. This environmentally benign protocol could provide a valuable synthetic method for practical applications.

Hetero-Diels-Alder reaction of [60]fullerene with nitrosoalkene

A new type of stable C60-fused dihydrooxazine derivatives was successfully prepared by the hetero-Diels-Alder reaction of C60 with nitrosoalkene generated in situ by extrusion of HBr from the corresponding α-bromooxime.

Insulinomimetic vanadyl-hydroxythiazolethione complexes with VO(S 2O2) coordination mode: The correlation between the activity and Hammett's substituent constant

Four kinds of vanadyl-hydroxythiazolethione complexes with VO(S 2O2) coordination mode were newly synthesized, and demonstrated for the first time that the insulinomimetic activity apparently correlates to the Hammett's substituent c