793-07-7

Usage

Uses

Used in Plastics Industry:
Benzoic acid,4,4'-(1,2-ethanediyl)bisis used as a plasticizer for various products, including cosmetics, personal care products, and pharmaceuticals. It enhances the flexibility and workability of plastics, making them easier to process and use.
Used in Perfumery:
As a solvent and fixative in perfumes, Benzoic acid,4,4'-(1,2-ethanediyl)bishelps to dissolve and stabilize the fragrance components, ensuring a longer-lasting and more consistent scent.
Used in Denaturation of Ethyl Alcohol:
Benzoic acid,4,4'-(1,2-ethanediyl)bisis used as a denaturant for ethyl alcohol, making it unsuitable for consumption and reducing the risk of accidental ingestion.
Used in Cellulose Acetate Solutions:
It serves as a solvent for cellulose acetate, which is used in the production of films, sheets, and extruded products. This allows for the creation of a wide range of products with specific properties and applications.
Used in Pesticide Formulations:
Benzoic acid,4,4'-(1,2-ethanediyl)biscan be used as a pesticide, helping to control and prevent the growth of unwanted organisms in various settings.
Used in Film, Sheet, and Extruded Product Manufacturing:
It plays a role in the production of films, sheets, and extruded products by acting as a plasticizer and solvent, contributing to the desired properties and performance of these materials.

Upstream product

• 4381-02-6 1,2-bis-(4-cyanophenyl)ethane 
• 99-94-5 p-Toluic acid 
• 79-37-8 oxalyl dichloride 
• 103-29-7 1,1'-(1,2-ethanediyl)bisbenzene 
• 797-21-7 1,2-bis(4-methoxycarbonylphenyl)ethane 
• 104-85-8 para-methylbenzonitrile 
• 1642-81-5 p-(chloromethyl)benzoic acid 
• 793-06-6 4,4'-diacetylbibenzyl 
• 6232-88-8 4-bromomethylbenzoic Acid 

Downstream Products

• 797-21-7 1,2-bis(4-methoxycarbonylphenyl)ethane 
• 119806-03-0 Bibenzyl-4,4'-dicarboxylic acid dichloride 
• 100-21-0 terephthalic acid 
• 116973-16-1 4,4'-bis-(α-hydroxy-benzhydryl)-bibenzyl 
• 88579-94-6 {4-[2-(4-hydroxymethyl-phenyl)ethyl]phenyl}methanol 
• 6337-67-3 4,4'-bis(bromomethyl)bibenzyl 
• 1633-22-3 [2.2]Paracyclophan 

Relevant academic research and scientific papers

Postsynthetic bromination of UiO-66 analogues: Altering linker flexibility and mechanical compliance

A new member of the UiO-66 series of zirconium metal-organic frameworks (MOFs) is reported, and the postsynthetic bromination of its integral alkene moeities in a single-crystal to single-crystal manner is fully characterised. Nanoindentation is used to p

Reactivity control of a photocatalytic system by changing the light intensity

We report a novel light-intensity dependent reactivity approach allowing us to selectively switch between triplet energy transfer and electron transfer reactions, or to regulate the redox potential available for challenging reductions. Simply by adjusting the light power density with an inexpensive lens while keeping all other parameters constant, we achieved control over one- and two-photon mechanisms, and successfully exploited our approach for lab-scale photoreactions using three substrate classes with excellent selectivities and good product yields. Specifically, our proof-of-concept study demonstrates that the irradiation intensity can be used to control (i) the available photoredox reactivity for reductive dehalogenations to selectively target either bromo- or chloro-substituted arenes, (ii) the photochemical cis-trans isomerization of olefins versus their photoreduction, and (iii) the competition between hydrogen atom abstraction and radical dimerization processes.

Reductive Homocoupling of Organohalides Using Nickel(II) Chloride and Samarium Metal

A homocoupling method for organohalides and organosulfonates promoted by samarium metal and HMPA, and catalyzed by NiCl2 has been developed. Various organohalides (benzyl, aryl, heterocyclic, alkenyl and alkyl halides), α-haloacetophenones, and phenyl organosulfonates were tolerated, and the reaction afforded coupling products with high efficiency. Excellent chemoselectivity was exhibited between halides and other groups, such as ?COOH, ?NO2, halogen, heterocyclic ring, ester, and ketone groups. The stereoselectivity suggested that the reaction mechanism might involve an organosamarium species.

Synthesis and Properties of Diethyl 5,10-Dihetera-5,10-dihydroindenoindene-2,7-dicarboxylates

A series of six heterocyclic diesters 1b-6b containing all combinations of nitrogen, sulfur, and selenium has been prepared from a common precursor, diethyl 2,2'-dinitrostilbene-4,4'-dicarboxylate.Electrochemical analysis showed oxidation potential increases in the order NA liquid crystals.A new synthetic method leading to the indoloindazole ring system has been found.

Reaktionen mit Radikalanionen, IV. Synthese von Mono- und Diketonen aus Carboxyl- und α,β-ungesaettigten Carbonyl-Verbindungen

1,2-Diketones of the benzil type were obtained in the reaction of aromatic carboxylic compounds with lithium naphthalenide.The scope of this reaction was investigated. α,β-Unsaturated ketones yielded hydrodimerisation, hydrogenation and hydroxylation products.