1027392-50-2

Basic information

• Product Name: 4-biphenyl-4-yl-6-(4-chloro-phenyl)-2-oxo-cyclohex-3-enecarboxylic acid ethyl ester
• CAS NO: 1027392-50-2
• Molecular Weight: 430.931
• Mol File: 1027392-50-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4-biphenyl-4-yl-6-(4-chloro-phenyl)-2-oxo-cyclohex-3-enecarboxylic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 4-biphenyl-4-yl-6-(4-chloro-phenyl)-2-oxo-cyclohex-3-enecarboxylic acid ethyl ester(1027392-50-2)
• EPA Substance Registry System: 4-biphenyl-4-yl-6-(4-chloro-phenyl)-2-oxo-cyclohex-3-enecarboxylic acid ethyl ester(1027392-50-2)

Safety Data

• Hazardous Substances Data: 1027392-50-2(Hazardous Substances Data)

Upstream product

• 13662-60-7 4-Chloro-4'-phenylchalcone 
• 141-97-9 ethyl acetoacetate 
• 92-52-4 biphenyl 
• 92-91-1 biphenyl-4-acetaldehyde 

Downstream Products

• 861406-41-9 C₂₅H₂₂ClN₃O 
• 1027906-58-6 3-biphenyl-4-yl-5-(4-chloro-phenyl)-cyclohex-2-enone 

Relevant articles and documents

Synthesis and antibacterial activity of some 5-(4-biphenylyl)-7-aryl[3,4-d] [1,2,3]-benzothiadiazoles

A series of 5-(4-biphenylyl)-7-aryl[3,4-d] [1,2,3]-benzothiadiazoles were synthesized, characterized by IR, NMR and elemental analysis and evaluated for in vitro antibacterial activity against some Gram-positive and Gram-negative bacteria. The antibacterial data revealed that compounds 7a-j had better activity against tested Gram-positive organisms than the reference ciprofloxacin and norfloxacin. However, the compounds were nearly inactive against Gram-negative bacteria. Compound 7c and 7d were the most active compounds against Gram-positive bacteria.