24319-76-4

Upstream product

• 99-93-4 4-Hydroxyacetophenone 
• 403-42-9 1-(4-fluorophenyl)ethanone 
• 123-31-9 hydroquinone 

Downstream Products

• 1047677-43-9 3-(4-{4-[4-(2-ethoxycarbonyl-1-methylvinyl)phenoxy]phenoxy}phenyl)but-2-enoic acid ethyl ester 
• 1047677-27-9 C₃₂H₃₄O₈ 
• 1047677-45-1 C₂₆H₂₆O₈ 
• 1047677-44-0 3-(4-{4-[4-(3-hydroxy-1-methylpropenyl)phenoxy]phenoxy}phenyl)but-2-ene-1-ol 
• 53563-78-3 1,4-bis[4-(4-aminophenoxy)phenoxy]benzene 
• 15051-26-0 4,4'-(1,4-phenylenebis(oxy)) diphenol 
• 83743-89-9 4,4'-(1,4-phenylenebis(oxy))bis(4,1-phenylene) diacetate 

Relevant academic research and scientific papers

EPOXY RESIN

The present disclosure relates to epoxide containing compounds comprising three benzene units linked by bridging groups. The disclosure also relates to the production of curable epoxy resin formulations comprising said epoxide containing compounds, and their possible incorporation into composite materials such as fibre reinforced composites. Possible methods for formulating the compounds epoxide containing compounds, as described herein, are also disclosed.

Thermal transition behaviors, solubility, and mechanical properties of wholly aromatic para -, meta -poly(ether-amide)s: Effect on numbers of para -aryl ether linkages

In order to make clear how the numbers of para-aryl ether linkages affect the solubility, thermal transition behavior and mechanical properties of para-(p-PEAs), meta-poly(ether-amide)s (m-PEAs), a series of para-substituted aryl ether diamine monomers with 2, 3, 4 or 5 ether linkages were synthesized, and then reacted with terephthalic acid and isophthalic acid via the Yamazaki-Higashi phosphorylation method to prepare wholly aromatic PEAs. The PEAs with intrinsic viscosity values in the range of 0.81-1.16 dL g-1 were obtained and characterized by FT-IR, NMR, and elemental analysis. Although the Tgs and Tms of PEAs decrease with the increasing numbers of aryl ether linkages, their Tgs and Tms still are above 180 °C and 320 °C, respectively. p-PEAs have a high crystallinity making it difficult to dissolve them in common organic solvents even when 5 aryl ether linkages are introduced. Conversely, except for m-PEA5 with a lower polarity, the other m-PEAs show good solubility due to their low crystallinity. Besides, the decomposition temperatures at 5% weight loss of all PEAs exceed 430 °C and their residual yields at 700 °C are above 50% in N2, illustrating that they have excellent thermal stability. It is found that by casting m-PEAs DMAc solution in a dish, the transparent films with high Young's modulus (2.6-3.5 GPa) can be successfully obtained.

A new approach to improving flame retardancy, smoke suppression and anti-dripping of PET: Via arylene-ether units rearrangement reactions at high temperature

In order to avoid the serious melt-dripping problems caused by conventional phosphorus flame retardants, a new arylene-ether containing monomer named 2,2′-(4,4′-(1,4-phenylenebis(oxy))bis(4,1-phenylene))bis(oxy) diethanol (PBPBD) was synthesized and intro

Facile regioselective synthesis of novel bis-thiazole derivatives and their antimicrobial activity

The design and synthesis of several new bis-thiazoles 4a-h serving as bis-drugs in comparison with mono-heterocyclic analogs are described. These bis-drugs present superior medicinal and pharmacological activities against both gram-negative (Pseudomonas a

Novel bis- and tris-1,2,4-trioxanes: Synthesis and antimalarial activity against multidrug-resistant Plasmodium yoelii in swiss mice

A new series of bis-1,2,4-trioxanes 12a-h, 13a-h, and 14a-h and tris-1,2,4-trioxanes 12i-14i were prepared and evaluated against multidrug-resistant Plasmodium yoelii in Swiss mice by oral route. Cyclopentane-based bis-trioxanes 12a, 12b, 12f-h and cycloh

NOVEL SUBSTITUTED BIS-1, 2, 4-TRIOXANES AND A PROCESS FOR PREPARATION THEREOF

The present invention relates to novel substituted bis-1, 2, 4-trioxanes i.e. compounds containing two 1, 2, 4-trioxane moieties of general formula (6) useful as antimalarial agents. This invention also relates to a process for the preparation of novel su

A convenient method for the preparation of 4-aryloxyphenols

A convenient method for the preparation of 4-aryloxyphenols via the homologation of preformed phenols is described. Condensation of various 4-substituted phenols with either 4-fluorobenzaldehyde (8) or 4-fluoroacetophenone (9) yielded the corresponding 4-aryl-oxybenzaldehydes, 10, and acetophenones, 11, in 70-93% yield. Baeyer-Villiger oxidation of these materials with 3-chloroperoxybenzoic acid (MCPBA) yielded the corresponding 4-formyloxy and 4-acetoxyphenyl ethers which were hydrolyzed without purification to the desired 4-aryloxyphenols 12 in 72-94% yield. Both 4-fluorobenzaldehyde (8) and 4-fluoroacetophenone (9) are synthetically equivalent to the a4 umpoled synthon 6. Extension of this methodology of the preparation of 4,4'-[arylbis(oxy)]bisphenols from aromatic diols is also described. Condensation of various aromatic diols with 8 or 9 yielded the corresponding 4,4'-[arylbis(oxy)]bisbenzaldehydes 15 and acetophenones 16 in 71-89% yield. Baeyer-Villiger oxidation of these compounds with MCPBA yielded the desired 4,4'-[arylbis(oxy)]bisphenyl bisformates 17 and bisacetates 18 in 67-84% yield. Hydrolysis of these compounds afforded the desired 4,4'-[arylbis(oxy)bisphenols 19 in 70-91% yield.