334709-76-1

Basic information

• Product Name: 2-BROMO-1-(4-FLUOROPHENYL)-1-ETHANONE OXIME
• Synonyms: 2-BROMO-1-(4-FLUOROPHENYL)-1-ETHANONE OXIME;2-bromo-1-(4-fluorophenyl)-1-ethanone oxime 97%;2-bromo-1-(4-fluorophenyl)-1-ethanoneoxime97%;(E)-2-broMo-1-(4-fluorophenyl)ethanone oxiMe
• CAS NO: 334709-76-1
• Molecular Formula: C8H7BrFNO
• Molecular Weight: 232.05
• Mol File: 334709-76-1.mol

Chemical Properties

• Melting Point: 84 °C
• Boiling Point: 291.6°C at 760 mmHg
• Flash Point: 130.2°C
• Appearance: /
• Density: 1.54g/cm³
• Vapor Pressure: 0.000882mmHg at 25°C
• Refractive Index: 1.554
• CAS DataBase Reference: 2-BROMO-1-(4-FLUOROPHENYL)-1-ETHANONE OXIME(CAS DataBase Reference)
• NIST Chemistry Reference: 2-BROMO-1-(4-FLUOROPHENYL)-1-ETHANONE OXIME(334709-76-1)
• EPA Substance Registry System: 2-BROMO-1-(4-FLUOROPHENYL)-1-ETHANONE OXIME(334709-76-1)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 334709-76-1(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
2-Bromo-1-(4-fluorophenyl)-1-ethanone oxime is utilized as a key intermediate in organic synthesis for the creation of various organic compounds. Its unique structure allows for further chemical reactions, making it a crucial component in the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-Bromo-1-(4-fluorophenyl)-1-ethanone oxime is employed as a starting material for the development of new drugs. Its potential applications in medicinal chemistry are vast, given its ability to be modified and incorporated into diverse drug candidates, which may lead to the discovery of novel therapeutic agents.
Used in Research and Development:
2-Bromo-1-(4-fluorophenyl)-1-ethanone oxime is also used in research and development settings to explore its chemical properties and reactivity. This helps in understanding its behavior in different chemical environments and can pave the way for innovative applications across various scientific disciplines.

InChI:InChI=1/C8H7BrFNO/c9-5-8(11-12)6-1-3-7(10)4-2-6/h1-4,12H,5H2/b11-8+

Upstream product

• 403-29-2 2-bromo-4'-fluoroacetophenone 
• 403-42-9 1-(4-fluorophenyl)ethanone 

Downstream Products

• 134516-39-5 dimethyl 3-(4-fluorophenyl)-1,2-oxazole-4,5-dicarboxylate 

Relevant articles and documents

α-Nitrosostyrenes as Three-Atom Units for the (3+1) Cyclization Reaction: Facile Access to 2,3-Dihydrodiazete N-Oxides and Their Diversified Synthetic Conversions

An unprecedented (3+1) cyclization of α-nitrosostyrenes, generated in situ from α-bromooximes, and N-tosyloxycarbamates was developed, which enables the synthesis of a range of structurally unique and hitherto unexplored 2,3-dihydrodiazete N-oxides in mod

Stereospecific synthesis and antimycobacterial activity of 1-aryl-2-(1H- imidazol-1-yl)-O-(aryl)-ethanoxime ethers E and Z oxiconazole analogs

A stereospecific synthesis of antifungal imidazolylarylethanoxime ether derivatives is reported. The (E) and (Z)- assignments, respectively, were made on the basis of 1H-NMR-spectral data. The new derivatives are provided with in vitro antimyco