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Usage

Uses

Used in Polymer and Plastics Industry:
1,3,5-tris(4-chlorophenyl)benzene is used as a monomer in the production of polymers and plastics, contributing to the formation of durable and versatile materials for various applications.
Used in Organic Synthesis:
1,3,5-tris(4-chlorophenyl)benzene is used as a starting material in the synthesis of various organic compounds, enabling the creation of a wide range of chemical products.
Used in Pharmaceutical Industry:
1,3,5-tris(4-chlorophenyl)benzene is used as an intermediate in the production of pharmaceuticals, playing a crucial role in the development of new drugs and medications.
Used in Agrochemical Industry:
1,3,5-tris(4-chlorophenyl)benzene is used as a precursor in the synthesis of agrochemicals, such as pesticides and herbicides, to help protect crops and enhance agricultural productivity.

Upstream product

• 141-52-6 sodium ethanolate 
• 99-91-2 para-chloroacetophenone 
• 873-73-4 4-n-chlorophenylacetylene 
• 403-42-9 1-(4-fluorophenyl)ethanone 

Relevant academic research and scientific papers

A simple Lewis acid induced reaction of phenols with electrophiles: Synthesis of functionalized 4H-chromenes and ortho-benzylphenols

Lewis acid ZnCl2 promoted cyclization protocol to 4H-chromenes is accomplished, using readily available phenols and acetophenones as starting materials. Interestingly, the process is feasible under the solvent free environment. Synthesis of a variety of 4H-chromenes have been accomplished using this strategy. In addition, this concept is extended to the synthesis of ortho-benzylphenols by treating phenols either with styrenes or secondary benzylic alcohols.

Zirconocene bis(perfluorooctanesulfonate) s-catalyzed highly efficient synthesis of 1,3,5-triaryl benzene via cyclotrimerization of ketones

Air-stable zirconocene bis(perfluoroctanesulfonate) s [Cp 2Zr]OSO2C8F17) 2] (1) with high Lewis acidity and high thermal stability was prepared by the reaction between Cp2ZrCl2 a

The highly selective formation of biaryls by the cyclization of arylethynes catalyzed by vanadyl phthalocyanine

The dimerization of arylethynes catalyzed by vanadium phthalocyanine to give substituted biaryls has been investigated. The reaction yield is always high and for many examples is only slightly affected by the aryl substituents. This fact is also related to the results obtained with metalloporphyrins, which give lower selectivities due to the presence of variable amounts of triphenylbenzenes.

A New Approach to the Stereoselective Synthesis of β-methylchalcones

Many β-methylchalcone derivatives have been prepared from self condensation of aralkyl ketones mediated by tetrachlorosilane-ethanol in mild conditions. - Key words: aralkyl ketones; tetrachlorosilane; β-methylchalcones; triarylbenzene derivatives