1353555-90-4

Basic information

• Product Name: 4-(4-(t-butyl)phenyl)-1-naphthaldehyde
• Synonyms: 4-(4-(t-butyl)phenyl)-1-naphthaldehyde
• CAS NO: 1353555-90-4
• Molecular Weight: 288.389
• Mol File: 1353555-90-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 4-(4-(t-butyl)phenyl)-1-naphthaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(4-(t-butyl)phenyl)-1-naphthaldehyde(1353555-90-4)
• EPA Substance Registry System: 4-(4-(t-butyl)phenyl)-1-naphthaldehyde(1353555-90-4)

Safety Data

• Hazardous Substances Data: 1353555-90-4(Hazardous Substances Data)

Upstream product

• 123324-71-0 p-tert-butylphenylboronic acid 
• 219685-17-3 trifluoromethanesulfonic acid 4-formylnaphthalen-1-yl ester 
• 7770-45-8 4-hydroxy-1-naphthaldehyde 

Downstream Products

• 1426170-83-3 C₂₁H₂₃N 
• 1431731-23-5 1-(azidomethyl)-4-(4-(t-butyl)phenyl)naphthalene 
• 1353555-93-7 (4-(4-(t-butyl)phenyl)naphthalen-1-yl)methanol 
• 1353554-83-2 C₂₂H₂₅N₃ 
• 1353555-94-8 1,3-di-Boc-2-((4-(4-(t-butyl)phenyl)naphthalen-1-yl)methyl)guanidine 
• 1353554-82-1 C₂₃H₂₇N₃ 
• 1353555-92-6 1,3-di-Boc-2-(2-(4-(4-(t-butyl)phenyl)naphthalen-1-yl)ethyl)guanidine 
• 1353554-81-0 C₂₂H₂₅N 
• 1353555-91-5 1-(4-(t-butyl)phenyl)-4-(2-nitrovinyl)naphthalene 

Relevant articles and documents

Antimicrobial activity of various 4- and 5-substituted 1-phenylnaphthalenes

Bacterial cell division occurs in conjunction with the formation of a cytokinetic Z-ring structure comprised of FtsZ subunits. Agents that can disrupt Z-ring formation have the potential, through this unique mechanism, to be effective against several of the newly emerging multi-drug resistant strains of infectious bacteria. 1- and 12-Aryl substituted benzo[c]phenanthridines have been identified as antibacterial agents that could exert their activity by disruption of Z-ring formation. Substituted 4- and 5-amino-1-phenylnaphthalenes represent substructures within the pharmacophore of these benzo[c] phenanthridines. Several 4- and 5-substituted 1-phenylnaphthalenes were synthesized and evaluated for antibacterial activity against Staphylococcus aureus and Enterococcus faecalis. The impact of select compounds on the polymerization dynamics of S. aureus FtsZ was also assessed.