118468-33-0

Usage

Chemical Properties

white fluffy powder

Upstream product

• 25934-47-8 1,2-bis-decyloxy-benzene 
• 75-36-5 acetyl chloride 
• 112-29-8 1-bromo dodecane 
• 1197-09-7 1-(3,4-dihydroxyphenyl)ethan-1-one 
• 2050-77-3 Iododecane 
• 120-80-9 benzene-1,2-diol 

Downstream Products

• 352432-33-8 1,2-bis(decyloxy)-4-ethynyl-benzene 
• 118468-32-9 tetradecyloxy-3,4,3',4' chalcone 

Relevant academic research and scientific papers

Synthesis and characterization of a new class of liquid-crystalline, highly luminescent molecules containing a 2,4,6-triphenyl-1,3,5-triazine unit

A new class of 2,4,6-triphenyl-1,3,5-triazine derivatives having long alkoxyl side chains have been synthesized by a Pd(0)/Cu(I)-catalyzed carbon-carbon coupling reaction. These compounds behave as liquid-crystalline materials and show quantum yields high

Substituent effects at the benzyl position and aromatic ring of silane-coupling agents containing 2-nitrobenzyl esters on photosensitivity and hydrophobic surface of a self-assembled monolayer (SAM)

Silane-coupling agents with 2-nitrobenzyl esters containing alkyl substituents at the benzyl position and alkoxy and/or fluoroalkoxy groups of the aromatic ring were synthesized to prepare a self-assembled monolayer (SAM) on quartz glass, silicon wafer and thermally oxidized silicon wafer. The resulting photosensitive SAMs before and after photoirradiation were characterized by contact angle measurement, UV spectroscopy, X-ray photoelectron spectroscopy (XPS), and X-ray reflectivity (XRR). Photosensitivity of the SAM was influenced by substituents at the benzyl position and aromatic ring as well as the irradiation conditions in air or solution and substrates employed. Silane-coupling agents with bulky substituent at the benzyl position and double fluoroalkoxy chains are preferable in terms of the photosensitivity and hydrophobic surface.

PREMIERS EXEMPLES DE SELS HETEROAROMATIQUES A QUATRE CHAINES PARAFFINIQUES POSSEDANT DES PROPRIETES MESOMORPHES COLONNAIRES

Homologous series of diaryl-3,5 dithiolium-1,2 and diaryl-2,6 pyrylium salts, in which aryls possess two flexible alkoxy chains, were synthesized.With n>=8, dithiolium salts exhibit a columnar hexagonal mesophase.