55792-66-0

Basic information

• Product Name: Acetamide, N-[4-(nonyloxy)phenyl]-
• CAS NO: 55792-66-0
• Molecular Formula: C17H27NO2
• Molecular Weight: 277.407
• Mol File: 55792-66-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Acetamide, N-[4-(nonyloxy)phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Acetamide, N-[4-(nonyloxy)phenyl]-(55792-66-0)
• EPA Substance Registry System: Acetamide, N-[4-(nonyloxy)phenyl]-(55792-66-0)

Safety Data

• Hazardous Substances Data: 55792-66-0(Hazardous Substances Data)

Upstream product

• 693-58-3 1-Bromononane 
• 103-90-2 4-acetaminophenol 

Downstream Products

• 862097-82-3 4-(4-nonyloxyphenylazo)phenol 
• 50262-67-4 4-(nonyloxy)aniline 

Relevant articles and documents

Synthesis and mesomorphic properties of 2,4-bis(4′-n-pentyloxybenzoyloxy)- benzylidine-4″- n-alkoxyaniline

The synthesis and mesomorphic properties of a new series of 2,4-bis(4′-npentyloxybenzoyloxy)- benzylidine-4″ -n-alkoxyaniline (DC5An) are reported. The molecular structure of compounds was confirmed by FTIR, 1H-NMR, 13C-NMR, mass spectroscopy and elemental analysis. The mesomorphic properties were studied by differential scanning calorimetry (DSC) and polarizing optical microscopy (POM) measurements. All compounds of the series exhibit nematic (N) and smectic C (SmC) phases. The first four homologues (DC5A1-DC5A4) display a N mesophase, whereas the highest homologues (DC5A5-DC5A10) exhibit an enantiotropic dimorphism N and SmC phases. The mesomorphic properties of the present series are compared and discussed with other structurally related series.

Electro-optical switching studies on 1,3-phenylene based banana shaped liquid crystals

This work deals with the study of the thermotropic liquid crystalline properties of new asymmetric bent core liquid crystals. The thermotropic properties was analyzed by polarized optical microscopy, differential scanning calorimetric analysis and variable temperature X-ray diffraction measurements. Effect of equal terminal chain with asymmetric bent core system on mesomorphic behavior was examined. The shorter methyl chain compound 10a of exhibits B 1 mesophase and higher homologs (10b and 10c) shows antiferroelectric B2 mesophases, which was studied by electro-optical measurements.

Mesogenicity of organophosphazenes: The effect of phosphazene rings and side groups on the phase transition

Cyclotriphosphazene and cyclotetraphosphazene derivatives with mesogenic 4-N-(4-alkoxyphenyl)iminomethyl)phenoxy and 4-(4′-alkoxy) biphenoxy moieties were synthesized. Schiff base moiety has higher mesomorphic stability than that in biphenyl moiety both in cyclotriphosphazene and cyclotetraphosphazene. Cyclotriphosphazenes possess higher thermal stability in the mesomorphic phase than the cyclotetraphosphazenes, suggesting the difference in the molecular structure.