605-01-6

Usage

Uses

Used in Chemical Synthesis:
Pentaethylbenzene is used as a chemical intermediate for the production of dyes and pharmaceuticals, contributing to the synthesis of a variety of compounds that have diverse applications in different industries.
Used in Industrial Applications:
Pentaethylbenzene is utilized as a solvent in various industrial processes, facilitating the dissolution of substances and aiding in the efficiency of manufacturing operations.
Used in Environmental and Health Safety:
While Pentaethylbenzene is a valuable chemical intermediate and solvent, it is also recognized as a hazardous substance. As such, it is used in the development of safety protocols and handling procedures to minimize its potential harmful effects on the environment and human health.

InChI:InChI=1/C16H26/c1-6-12-11-13(7-2)15(9-4)16(10-5)14(12)8-3/h11H,6-10H2,1-5H3

Upstream product

• 42205-08-3 1,2,3-triethylbenzene 
• 74-96-4 ethyl bromide 
• 71-43-2 benzene 
• 74-85-1 ethene 
• 75-00-3 chloroethane 
• 77922-78-2 pentaethylacetophenone 
• 7446-70-0 aluminium trichloride 
• 604-88-6 hexaethylbenzene 
• 10034-85-2 hydrogen iodide 
• 7664-93-9 sulfuric acid 
• 63877-66-7 pentaethyl-benzenesulfonic acid 
• 504-61-0 (E)-but-2-enol 
• 928-49-4 hex-3-yne 
• 598-32-3 2-hydroxy-3-butene 

Downstream Products

• 642-32-0 1,2,3,4-tetraethylbenzene 
• 4681-81-6 2,3,4,5-tetraethylbenzene sulfonic acid 
• 63877-66-7 pentaethyl-benzenesulfonic acid 
• 77922-77-1 1,2,4,5-tetraethyl-3,6-dinitro-benzene 
• 102020-25-7 1-pentaethylphenyl-propan-1-one 
• 77922-78-2 pentaethylacetophenone 
• 18780-09-1 2-chloro-1-pentaethylphenyl-ethanone 
• 20020-99-9 Nitropentaaethylbenzol 
• 604-88-6 hexaethylbenzene 
• 908100-24-3 1,2,3,4-tetraethyl-5,6-dinitro-benzene 
• 860511-91-7 pentaethyl-benzenesulfonyl chloride 
• 858241-75-5 3,4,5,6-tetraethyl-o-phenylenediamine 
• 92299-36-0 1,2-dibromo-3,4,5,6-tetraethylbenzene 
• 92298-60-7 1,2,3,4-tetraethyl-5-bromo-benzene 

Relevant academic research and scientific papers

Process for the production of alkylaromatics

A process for producing an alkylaromatic compound includes contacting a dilute olefin feed with a lean oil stream containing aromatic compound and alkylaromatic compound in an absorption zone to provide an alkylation reaction stream containing aromatic co

Palladium-catalyzed benzannulation from alkynes and allylic compounds

Various alkynes reacted with allyl tosylates in the presence of palladium catalysts, giving polysubstituted benzenes with good to high regioselectivity. Pentasubstituted and trisubstituted benzenes were readily prepared by reaction of internal alkynes and

Charge-transfer probes for molecular recognition via steric hindrance in donor-acceptor pairs

Molecular association of various aromatic hydrocarbons (D, including sterically hindered donors) with a representative group of diverse acceptors (A = quinone, trinitrobenzene, tetracyanoethylene, tropylium, tetranitromethane, and nitrosonium) is visually apparent in solution by the spontaneous appearance of distinctive colors. Spectral (UV-vis) analyses of the colored solutions reveal their charge-transfer origin (λ(CT)) and they provide quantitative information of the intermolecular association in the form of the K(DA) and ε(CT) values for the formation and visualization, respectively, of different [D,A] complexes. Importantly, such measurements establish charge-transfer absorption to be a sensitive analytical tool for evaluating the steric inhibition of donor-acceptor association. For example, the steric differences among various hindered aromatic donors in their association with quinone are readily dramatized in their distinctive charge-transfer (color) absorptions and verified by X-ray crystallography of the charge-transfer crystals and/or QUANTA molecular modeling calculations of optimum intermolecular separations allowed by van der Waals contacts.