55476-93-2

Basic information

• Product Name: Ethanone, 2-bromo-2-(4-chlorophenoxy)-1-phenyl-
• CAS NO: 55476-93-2
• Molecular Formula: C14H10BrClO2
• Molecular Weight: 325.589
• Mol File: 55476-93-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Ethanone, 2-bromo-2-(4-chlorophenoxy)-1-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 2-bromo-2-(4-chlorophenoxy)-1-phenyl-(55476-93-2)
• EPA Substance Registry System: Ethanone, 2-bromo-2-(4-chlorophenoxy)-1-phenyl-(55476-93-2)

Safety Data

• Hazardous Substances Data: 55476-93-2(Hazardous Substances Data)

Upstream product

• 18859-48-8 2-(4-chlorophenoxy)-1-phenylethanone 

Downstream Products

• 24257-90-7 phenyl-glyoxal-bis-(4-nitro-phenylhydrazone) 
• 161498-76-6 2-(4-Chloro-phenoxy)-2-[5-(2-hydroxy-phenyl)-4-phenylamino-4H-[1,2,4]triazol-3-ylsulfanyl]-1-phenyl-ethanone 
• 161498-77-7 2-(4-Chloro-phenoxy)-2-[5-(4-hydroxy-phenyl)-4-phenylamino-4H-[1,2,4]triazol-3-ylsulfanyl]-1-phenyl-ethanone 
• 161498-78-8 2-(4-Chloro-phenoxy)-2-(5-methyl-4-phenylamino-4H-[1,2,4]triazol-3-ylsulfanyl)-1-phenyl-ethanone 
• 129330-21-8 7-(4-Chloro-phenoxy)-3,6-diphenyl-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazine 
• 129330-16-1 7-(4-Chloro-phenoxy)-3-ethyl-6-phenyl-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazine 
• 129330-11-6 7-(4-Chloro-phenoxy)-3-methyl-6-phenyl-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazine 
• 92874-03-8 1-(4-chlorophenoxy)-2-oxo-2-phenylethyl acetate 
• 161498-75-5 2-(4-Chloro-phenoxy)-1-phenyl-2-(5-phenyl-4-phenylamino-4H-[1,2,4]triazol-3-ylsulfanyl)-ethanone 

Relevant articles and documents

Synthesis of Some New Biologically Active 5-Phenoxy-4-phenyl-1,3-thiazol-2-amines.

Several new 5-phenoxy-4-phenyl-1,3-thiazol-2-amines have been synthesised via Hantzsch's synthesis and some of these thiazoles have been screened for their in vitro antibacterial activity.

α-Haloalkyl Ethers in Alkylations of 2-Pyrimidinones

The ambident 5-halopyrimidin-2-one anion with potassium as counterion in DMF is preferentially O-alkylated using the relatively hard α-chloroalkyl ether electrophiles.As ammonium salts in dichloromethane or by the use of KF-alumina in DME the preference is for N-alkylation.TMS ethers of the pyrimidinones are exclusively N-alkylated.