1166917-93-6

Basic information

• Product Name: 3,4,5-tris(dodecyloxy)-N-(4-ethynylphenyl)benzamide
• Synonyms: 3,4,5-tris(dodecyloxy)-N-(4-ethynylphenyl)benzamide
• CAS NO: 1166917-93-6
• Molecular Weight: 774.224
• Mol File: 1166917-93-6.mol

Chemical Properties

• CAS DataBase Reference: 3,4,5-tris(dodecyloxy)-N-(4-ethynylphenyl)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4,5-tris(dodecyloxy)-N-(4-ethynylphenyl)benzamide(1166917-93-6)
• EPA Substance Registry System: 3,4,5-tris(dodecyloxy)-N-(4-ethynylphenyl)benzamide(1166917-93-6)

Safety Data

• Hazardous Substances Data: 1166917-93-6(Hazardous Substances Data)

Upstream product

• 540-37-4 p-aminoiodobenzene 
• 75867-39-9 4-trimethylsilylethynyl aniline 
• 14235-81-5 4-Ethynylaniline 
• 117241-31-3 3,4,5-tridodecyloxy benzoic acid 
• 149-91-7 3,4,5-trihydroxybenzoic acid 
• 831-61-8 Ethyl gallate 
• 117241-30-2 ethyl 3,4,5-tri(dodecyloxy)benzoate 
• 1407974-60-0 3,4,5-tris(dodecyloxy)-N-(4-iodophenyl)benzamide 
• 123126-39-6 methyl [3,4,5-tris(n-dodecan-1-yloxy)]benzoate 
• 99-24-1 methyl galloate 
• 143-15-7 1-dodecylbromide 

Downstream Products

• 1443989-84-1 C₆₇H₁₀₁NO₅Si 
• 1447923-83-2 C₆₃H₁₁₂INO₄P₂Pt 
• 1459809-74-5 C₁₁₄H₁₉₄N₂O₈P₂Pt 
• 1417796-60-1 C₁₄₆H₂₃₂N₂O₈P₄Pt₂ 
• 1417796-61-2 C₁₄₆H₂₃₂N₂O₈P₄Pt₂ 
• 1417796-53-2 C₇₄H₁₁₆O₃P₂Pt 

Relevant articles and documents

Influence of functional groups on the self-assembly of liquid crystals

Functional groups in the molecule play an important role in the molecular organization process. To reveal the influence of functional groups on the self-assembly at interface, herein, the self-assembly structures of three liquid crystal molecules, which only differ in the functional groups, are explicitly characterized by using scanning tunneling microscopy (STM). The high-resolution STM images demonstrate the difference between the supramolecular assembly structures of three liquid crystal molecules, which attribute to the hydrogen bonding interaction and π-π stacking interaction between different functional groups. The density functional theory (DFT) results also confirm the influence of these functional groups on the self-assemblies. The effort on the self-assembly of liquid crystal molecules at interface could enhance the understanding of the supramolecular assembly mechanism and benefit the further application of liquid crystals.

Influence of Ester versus Amide Linkers on the Supramolecular Polymerization Mechanisms of Planar BODIPY Dyes

We report the H-type supramolecular polymerization of two new hydrophobic BODIPY derivatives equipped with ester and amide linkages. Whereas the ester-containing BODIPY derivative undergoes an isodesmic supramolecular polymerization in which the monomers are parallel-oriented, the replacement of the ester by amide groups leads to a highly cooperative self-assembly process into H-type aggregates with a rotational displacement of the dye molecules within the stack. The dye organization imposed by simultaneous π–π and hydrogen bonding interactions is the driving force for the cooperative supramolecular polymerization, whereas the absence of additional hydrogen bonds for the ester-containing moiety does not suffice to induce cooperative phenomena.

Cooperative self-assembly of platinum(ii) acetylide complexes

Rod-like platinum(ii) acetylide complexes have been demonstrated to form one-dimensional helical supramolecular polymers by the cooperative growth mechanism, leading to supramolecular gels by bundling single fibrils into entangled networks.