1329426-08-5

Basic information

• Product Name: 4,4,5,5-tetramethyl-2-(3,4,5-tris-(n-octyloxy)phenyl)-1,3,2-dioxaborolane
• Synonyms: 4,4,5,5-tetramethyl-2-(3,4,5-tris-(n-octyloxy)phenyl)-1,3,2-dioxaborolane
• CAS NO: 1329426-08-5
• Molecular Weight: 588.72
• Mol File: 1329426-08-5.mol

Chemical Properties

• CAS DataBase Reference: 4,4,5,5-tetramethyl-2-(3,4,5-tris-(n-octyloxy)phenyl)-1,3,2-dioxaborolane(CAS DataBase Reference)
• NIST Chemistry Reference: 4,4,5,5-tetramethyl-2-(3,4,5-tris-(n-octyloxy)phenyl)-1,3,2-dioxaborolane(1329426-08-5)
• EPA Substance Registry System: 4,4,5,5-tetramethyl-2-(3,4,5-tris-(n-octyloxy)phenyl)-1,3,2-dioxaborolane(1329426-08-5)

Safety Data

• Hazardous Substances Data: 1329426-08-5(Hazardous Substances Data)

Upstream product

• 73183-34-3 bis(pinacol)diborane 
• 16492-75-4 5-bromo-1,2,3 trihydroxybenzene 
• 2675-79-8 1-bromo-3,4,5-trimethoxybenzene 
• 61676-62-8 2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 

Downstream Products

• 1329426-13-2 2,4,6-tris[5-(3,4,5-trioctyloxyphenyl)thiophen-2-yl]-1,3,5-triazine 
• 1451050-10-4 C₇₁H₁₀₉BF₆N₂O₈ 
• 1451050-11-5 1,3-bis[3,4-difluoro-5-(3,4,5-trioctyloxyphenyl)pyrrol-2-yl]-1,3-propanedi-one 

Relevant articles and documents

Ion-pair-based assemblies comprising pyrrole-pyrazole hybrids

Modified 3,5-dipyrrolylpyrazole (DPP) derivatives in their protonated form produce planar [2+2]-type complexes with trifluoroacetate (TFA) ions. These complexes serve as constituent components of ion-pair-based assemblies. An essential strategy for the co

Electro-functional octupolar π-conjugated columnar liquid crystals

A series of propeller-shaped π-conjugated molecules based on 2,4,6-tris(thiophene-2-yl)-1,3,5-triazines has been designed and synthesized to obtain ambipolar charge-transporting liquid-crystalline materials. The 3-fold electron-donating aromatic units are attached to the electron-accepting triazine core, which forms electro-functional octupolar π-conjugated structures. These octupolar molecules self-organize into one-dimensional columnar nanostructures and exhibit ambipolar carrier transport behavior, which has been revealed by time-of-flight measurements. In this approach, electron-donor and acceptor electro-active segments are assembled individually in each column to give one-dimensional nanostructured materials with precisely tuned electronic properties. Their desirable electronic structures responsible for both hole and electron conductions have also been examined by cyclic voltammetry and theoretical calculations. The present results provide a new guideline and versatile approach to the design of ambipolar conductive nanostructured liquid-crystalline materials.