13662-55-0

Upstream product

• 92-52-4 biphenyl 
• 92-91-1 biphenyl-4-acetaldehyde 
• 135-02-4 ortho-anisaldehyde 

Downstream Products

• 1027952-23-3 4-biphenyl-4-yl-6-(2-methoxy-phenyl)-2-oxo-cyclohex-3-enecarboxylic acid ethyl ester 
• 1027292-62-1 3-biphenyl-4-yl-5-(2-methoxy-phenyl)-cyclohex-2-enone 
• 861406-43-1 C₂₆H₂₅N₃O₂ 

Relevant academic research and scientific papers

SAR studies of differently functionalized 4′-phenylchalcone based compounds as inhibitors of cathepsins B, H and L

Conditions related to the elevated levels of cathepsin B [3.4.22.1], cathepsin H [3.4.22.16] and cathepsin L [3.4.22.15] in various cancerous, rheumatoid arthritis and tissue degenerative disorders motivate the design, synthesis and evaluation of compound

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.

Synthesis and antibacterial activities of some 2-amino-4,6- diarylpyrimidines

A series of 2-aminopyrimidines have been prepared by the condensation of 1-(1,1′-biphenyl-4-yl)-3-arylprop-2-en-1-ones with guanidine-nitrate and characterized on the basis of analytical and spectral data. The compounds have been screened for their antibacterial activities.