915779-75-8

Basic information

• Product Name: Benzonitrile, 4-(dodecyloxy)-2-(trifluoromethyl)-
• CAS NO: 915779-75-8
• Molecular Formula: C20H28F3NO
• Molecular Weight: 355.444
• Mol File: 915779-75-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzonitrile, 4-(dodecyloxy)-2-(trifluoromethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzonitrile, 4-(dodecyloxy)-2-(trifluoromethyl)-(915779-75-8)
• EPA Substance Registry System: Benzonitrile, 4-(dodecyloxy)-2-(trifluoromethyl)-(915779-75-8)

Safety Data

• Hazardous Substances Data: 915779-75-8(Hazardous Substances Data)

Upstream product

• 367-67-9 2-bromo-5-nitro-benzotrifluoride 
• 112-53-8 1-dodecyl alcohol 
• 320-47-8 4-nitro-2-trifluoromethylbenzonitrile 

Relevant articles and documents

Self-association of bis-dendritic organogelators: The effect of dendritic architecture on multivalent cooperative interactions

A series of bis-dendritic gelators consisting of a benzamide dendron and an alkyl dendron were synthesized to investigate the dendritic effect on self-assembly. The gelators with a firstgeneration benzamide (benzamide-G1) dendron or a first-generation alkyl (alkyl-G1) dendron formed stable gels in most aromatic solvents, and their self-assembled fibrillar networks were imaged by electron microscopy. The unbranched molecule (G0-G0) or the molecule possessing a second-generation benzamide (benzamide-G2) dendron did not form gels. Differential scanning calorimetry, powder X-ray diffraction, and Fourier transform IR studies revealed that introduction of a dendritic branch strongly affected the molecular packing as well as the strength of intermolecular interactions. Furthermore, concentration-dependent diffusion coefficient measurements and the evaluation of association constants by 1H NMR spectroscopy indicated that bis-dendritic gelators with a benzamide-G1 dendron possessed high association constants and formed large aggregates, whereas molecules with a single benzamide formed dimers in chloroform. The formation of self-assembled fibrillar networks was driven by the multivalent and cooperative hydrogen bonding observed in the benzamide- G1 dendrons. π- π stacking of aromatic groups and van der Waals interactions between alkyl chains also played roles in the self-assembly process, thus indicating that a spatial balance between two dendrons is important.

Molecular self-assembly of macroporous parallelogrammatic pipes

The pipes, the pipes are calling: Organic parallelogram-shaped pipes of micrometer dimensions have been obtained by simply allowing drops of a solution of low-molecular-weight compounds to evaporate. This unique structure is formed by self-templated crystal growth during the evaporation. The mechanism of formation involves two polymorphic crystal forms in dynamic nonequilibrium conditions. (Figure Presented).