14181-83-0

Basic information

• Product Name: Ethanone, 2-bromo-1-(4-methoxyphenyl)-, oxime
• CAS NO: 14181-83-0
• Molecular Formula: C9H10BrNO2
• Molecular Weight: 244.088
• Mol File: 14181-83-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Ethanone, 2-bromo-1-(4-methoxyphenyl)-, oxime(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 2-bromo-1-(4-methoxyphenyl)-, oxime(14181-83-0)
• EPA Substance Registry System: Ethanone, 2-bromo-1-(4-methoxyphenyl)-, oxime(14181-83-0)

Safety Data

• Hazardous Substances Data: 14181-83-0(Hazardous Substances Data)

Usage

General Description

Ethanone, 2-bromo-1-(4-methoxyphenyl)-, oxime is a chemical compound often used in organic synthesis and research. It belongs to the oxime class of compounds and is derived from the reaction of 2-bromo-1-(4-methoxyphenyl)ethanone with hydroxylamine. Ethanone, 2-bromo-1-(4-methoxyphenyl)-, oxime has potential applications in the pharmaceutical industry as it can be used as a starting material for the synthesis of various biologically active compounds. It may also have applications in the development of new drugs and can be used as a reagent in organic chemistry reactions. Additionally, it has the potential to be used in the agricultural industry as a crop protection agent. However, its toxicity and environmental impact need to be carefully evaluated before widespread use.

Upstream product

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

Downstream Products

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

Relevant articles and documents

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

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.

N-hydroxy-4-(p-chlorophenyl)thiazole-2(3H)-thione: [2(3H)-thiazolethione, 4-(4-chlorophenyl)-3-hydroxy-]

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