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Fluorobenzaldehyde can be used as a synthetic intermediate because the fluorine can be replaced via oxidation reaction. [1] Due to the aldehyde group, the fluorobenzaldehydes can be used to make a variety of schiff base compounds through a condensation reaction, some of which have antimicrobial properties. [2] [3]
Pentafluorobenzene is an organofluoride compound with the molecular formula C 6 HF 5. [1] The compound consists of a benzene ring substituted with five fluorine atoms. [2] The substance is a colorless liquid with a boiling point similar to that of benzene.
Substitution of fluoride occurs typically at the para position. This reaction has been used to anchor the −C 6 F 4 CO 2 H group to surfaces. Magnesium methoxide results in ortho methoxylation.
The generic formula of an azine. For an aldazine, R 2 = H. Azines are a functional class of organic compounds with the connectivity RR'C=N-N=CRR'. These compounds are the product of the condensation of hydrazine with ketones and aldehydes, although in practice they are often made by alternative routes. Ketazines are azines derived from ketones. [1]
Structure of [(C 5 Me 5) 2 Ti(FC 6 H 5)] +, a coordination complex of fluorobenzene.. PhF is a useful solvent for highly reactive species. Its melting point at -44 °C is lower than that of benzene.
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In Hantzsch–Widman nomenclature, an azine is an heterocyclic compound containing a 6-membered aromatic ring. It is an analog of a benzene ring in which one or more of the carbon atoms has been replaced by a nitrogen atom, [ 1 ] and thus is also called an azabenzene .
4-Trifluoromethylbenzaldehyde is the organofluorine compound with the formula CF 3 C 6 H 4 CHO.Two other isomers are also known: 2-trifluoromethylbenzaldehyde and 3-trifluoromethylbenzaldehyde.