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Benzocycloheptenes are cycloheptenes with additional benzene rings attached. Most have two benzene rings, and are called dibenzocycloheptenes.. Some benzocycloheptenes and substituted benzocycloheptenes have medical uses as antihistamines, anticholinergics, antidepressants, and antiserotonergics.
A heterocyclic compound or ring structure is a cyclic compound that has atoms of at least two different elements as members of its ring(s). [1] Heterocyclic organic chemistry is the branch of organic chemistry dealing with the synthesis, properties, and applications of organic heterocycles .
Dibenzo-1,4-dioxin, also known as dibenzodioxin or dibenzo-p-dioxin (molecular formula C 12 H 8 O 2), in which two benzene rings are connected through two oxygen atoms. That is the parent compound of the dioxins (see next in which the dioxins comprise a key part of the class).
Heteroarenes are aromatic compounds, where at least one methine or vinylene (-C= or -CH=CH-) group is replaced by a heteroatom: oxygen, nitrogen, or sulfur. [3] Examples of non-benzene compounds with aromatic properties are furan, a heterocyclic compound with a five-membered ring that includes a single oxygen atom, and pyridine, a heterocyclic compound with a six-membered ring containing one ...
The name dioxin formally refers to the central dioxygenated ring, which is stabilized by the two flanking benzene rings. In PCDDs, chlorine atoms are attached to this structure at any of 8 different places on the molecule, at positions 1–4 and 6–9. There are 75 different PCDD congeners (that is, related dioxin compounds). [7]
Many simple aromatic rings have trivial names. They are usually found as substructures of more complex molecules ("substituted aromatics"). Typical simple aromatic compounds are benzene, indole, and pyridine. [1] [2] Simple aromatic rings can be heterocyclic if they contain non-carbon ring atoms, for example, oxygen, nitrogen, or sulfur.
The C 2 benzenes are a class of organic aromatic compounds which contain a benzene ring and two other carbon atoms. For the hydrocarbons with no further unsaturation, there are four isomers. There are three xylenes and one ethylbenzene .
The following table shows a series of Gibbs free energy of binding between benzene and several cations in the gas phase. [ 2 ] [ 6 ] For a singly charged species, the gas-phase interaction energy correlates with the ionic radius , r i o n {\displaystyle r_{\mathrm {ion} }} (non-spherical ionic radii are approximate).