162709-82-2

Basic information

• Product Name: Benzene, 5-(chloromethyl)-1,2,3-tris(octyloxy)-
• CAS NO: 162709-82-2
• Molecular Formula: C31H55ClO3
• Molecular Weight: 511.229
• Mol File: 162709-82-2.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzene, 5-(chloromethyl)-1,2,3-tris(octyloxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 5-(chloromethyl)-1,2,3-tris(octyloxy)-(162709-82-2)
• EPA Substance Registry System: Benzene, 5-(chloromethyl)-1,2,3-tris(octyloxy)-(162709-82-2)

Safety Data

• Hazardous Substances Data: 162709-82-2(Hazardous Substances Data)

Upstream product

• 629-27-6 1-Iodooctane 
• 342886-36-6 3,4,5-tris(octyloxy)benzoic acid methyl ester 
• 99-24-1 methyl galloate 
• 111-83-1 1-bromo-octane 
• 342886-38-8 (3,4,5-tris-octyloxy-phenyl)-methanol 
• 157980-10-4 ethyl 3,4,5-tris(octyloxy)benzoate 

Downstream Products

• 1221072-20-3 C₃₁H₅₅N₃O₃ 
• 957336-60-6 1-methyl-3-[3,4,5-tris(octyloxy)benzyl]imidazolium bis(trifluoromethylsulfonyl)imide 
• 1193467-65-0 C₁₀₁H₁₇₀O₁₄ 
• 1041170-54-0 C₃₇H₅₉IO₄ 

Relevant articles and documents

Synthesis and characterization of α-cyanostilbene-based bent-core hexacatenar mesogens with different central groups

Two series of bent-core hexacatenars containing a diphenyl ketone/diphenylmethylene malononitrile as central group and two α-cyanostilbene units as molecular arm were synthesized by Suzuki coupling and Knoevenagel reactions. The effect of the central groups on the liquid crystalline and photophysical behaviors was investigated in detail. POM, DSC and XRD results indicated that all the compounds could self-assemble into hexagonal columnar mesophases and diphenylmethylene malononitrile-based hexacatenars show much wider range of mesophase. The introduction of malononitrile unit into aromatic core could induce more distinct solvatochromic effect. Both series of hexacatenars show aggregation-induced emission enhancement (AIEE) behaviors and the fluorescence intensity is affected by the size of spherical aggregates in the aggregated state. Additionally, the maximum emission bands, fluorescence intensity and fluorescence color in condensed state showed obvious transition upon rising temperature.

Coumarin-based emissive hexacatenars: synthesis, 2D and 3D self-assembly and photodimerization

The first examples of unsymmetric coumarin polycatenar liquid crystals consisting of a coumarin central core with 1,2,3-triazole dendritic wings on both sides were synthesized via click reaction. Their properties were investigated using POM, DSC, XRD, SEM

Synthesis and characterization of room temperature columnar mesogens of cyclotriphosphazene with Schiff base units

New supermolecular liquid crystals have been synthesized by attaching polycatenar aromatic units with three terminal alkyl chains through imine linking groups to a central cyclotriphosphazene ring, and these were investigated by polarizing microscopy, DSC