771477-09-9

Basic information

• Product Name: N-[4-(2-fluoro-4-nitrophenoxy)phenyl]acetamide
• CAS NO: 771477-09-9
• Molecular Weight: 290.251
• Mol File: 771477-09-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-[4-(2-fluoro-4-nitrophenoxy)phenyl]acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-[4-(2-fluoro-4-nitrophenoxy)phenyl]acetamide(771477-09-9)
• EPA Substance Registry System: N-[4-(2-fluoro-4-nitrophenoxy)phenyl]acetamide(771477-09-9)

Safety Data

• Hazardous Substances Data: 771477-09-9(Hazardous Substances Data)

Upstream product

• 369-34-6 3,4-difluoronitrobenzene 
• 103-90-2 4-acetaminophenol 

Downstream Products

• 771477-17-9 Methanesulfonic acid (R)-3-[4-(4-acetylamino-phenoxy)-3-fluoro-phenyl]-2-oxo-oxazolidin-5-ylmethyl ester 
• 771477-25-9 N-{4-[2-fluoro-4-(5-isothiocyanatomethyl-2-oxo-oxazolidin-3-yl)-phenoxy]-phenyl}-acetamide 
• 771477-13-5 benzyl 4-[4-(acetylamino)phenoxy]-3-fluorophenylcarbamate 
• 771477-19-1 N-(4-{4-[(5R)-5-(azidomethyl)-2-oxo-1,3-oxazolidin-3-yl]-2-fluorophenoxy}phenyl)acetamide 
• 771477-21-5 N-(4-{4-[(5S)-5-(aminomethyl)-2-oxo-1,3-oxazolidin-3-yl]-2-fluorophenoxy}phenyl)acetamide 
• 771477-15-7 N-(4-{2-fluoro-4-[(5R)-5-(hydroxymethyl)-2-oxo-1,3-oxazolidin-3-yl]phenoxy}phenyl)acetamide 
• 771477-11-3 N-[4-(4-amino-2-fluoro-phenoxy)-phenyl]-acetamide 

Relevant articles and documents

Synthesis and antibacterial activity of some aryloxy/thioaryloxy oxazolidinone derivatives

A series of aryloxy/thioaryloxy oxazolidinones has been synthesized and their antibacterial activity in vitro were evaluated and compared with linezolid. A series of aryloxy/thioaryloxy oxazolidinone derivatives has been synthesized and tested for in vitro antibacterial activity by MIC determination against a panel of susceptible and resistant Gram-positive and Gram-negative microorganisms, some of which are resistant to methicillin and vancomycin. Compounds 12a, 12b, 14a, and 14b from this series were found to be equipotent or more potent than linezolid in vitro.