The phrase "aryl compound" is correct and usable in written English.
It is typically used in the context of chemistry to refer to a compound that contains an aromatic ring structure.
Example: "The researchers synthesized a new aryl compound that showed promising results in their experiments."
Alternatives: "aromatic compound" or "phenyl compound".
In the wild type protein, N102 formed weak hydrogen bonds to the 1,4-dihydroxy aryl compound (dotted line) which were lost upon mutation to a serine residue.
Docking simulations were compared using models of wild type and SCD mutant (N102S) UBIAD1 protein and substrates, farnesyldiphosphate and a 1,4-dihydroxy aryl compound (Figure 6D and 6E).
As shown in Figure 8e the aryl compound 24 predicted to bind in a forward binding mode while the fluorenyl analog 26 binds in the reverse binding mode (Figure 8f) with extended interactions in HBP3s and HBP1s respectively.
The epoxides (oxiranes) have been a major topic of interest with olefins and aryl compounds.
(2009) describe a synthetic chemistry method to produce specifically fluorinated aryl compounds from aryl triflates under mild reaction conditions and in a single step.
Chemists have been trying to find a widely applicable catalytic method to attach CF3 to aryl compounds (compounds containing one or more six-carbon rings) for a couple of decades.
Some have achieved different parts of the reaction, but none successfully put all the pieces together to arrive at a method that is applicable for a wide range of different aryl compounds.
The electroreduction of several dihalogenated aryl compounds was carried out in the presence of pinacolborane as the electrophile for the synthesis of halogenated arylboronic ester derivatives.
There is more than one idealised bond angle for sd3, sd4 and sd5 hybrids which correlates with the irregular geometries found for hydride, alkyl and aryl compounds.
A series of 10 thiourea derivatives have been synthesized by the reaction of aromatic amine with a substituted aryl (compounds 1 3, 6 8) and alkylphenyl (4, 5, 9, 10) isothiocyanates.
Fortunately, electron impact mass spectrometry, by which abundant fragment ions can be obtained, is a useful and straightforward method to identify the (poly)aryl compounds [11 16].
