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	<title>Fluorobenzene - Revision history</title>
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	<updated>2026-04-26T21:44:18Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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		<id>https://wikimd.org/index.php?title=Fluorobenzene&amp;diff=5607604&amp;oldid=prev</id>
		<title>Prab: CSV import</title>
		<link rel="alternate" type="text/html" href="https://wikimd.org/index.php?title=Fluorobenzene&amp;diff=5607604&amp;oldid=prev"/>
		<updated>2024-04-15T16:43:45Z</updated>

		<summary type="html">&lt;p&gt;CSV import&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;[[Image:Cp*Ti(FPh)+.png|thumb]]    &amp;#039;&amp;#039;&amp;#039;Fluorobenzene&amp;#039;&amp;#039;&amp;#039; is an [[organic compound]] with the formula C&amp;lt;sub&amp;gt;6&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;5&amp;lt;/sub&amp;gt;F. This [[fluoroaromatic]] compound is a colorless, flammable liquid that is used in the chemical industry as a solvent and in the manufacture of other chemicals. Fluorobenzene is structurally related to [[benzene]], with one of the hydrogen atoms replaced by a [[fluorine]] atom. This substitution significantly alters the chemical properties of the compound, making it less reactive than benzene. It is an important intermediate in the production of pharmaceuticals and agrochemicals.&lt;br /&gt;
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==Properties==&lt;br /&gt;
Fluorobenzene has a boiling point of approximately 85°C and a melting point of -42°C. It is slightly soluble in [[water]], but it is miscible with many organic solvents such as [[ethanol]], [[diethyl ether]], and [[benzene]]. The presence of the fluorine atom on the benzene ring affects the electron distribution within the molecule, which influences its reactivity and physical properties.&lt;br /&gt;
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==Production==&lt;br /&gt;
Fluorobenzene is typically produced through the [[halogenation]] of benzene, using sources of fluorine such as [[sulfur tetrafluoride]] (SF&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;) or [[cobalt(III) fluoride]] (CoF&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;). The process involves the substitution of a fluorine atom for a hydrogen atom on the benzene ring. This reaction requires careful control of conditions to ensure selectivity for the monofluorinated product.&lt;br /&gt;
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==Applications==&lt;br /&gt;
Fluorobenzene is used as a solvent in the chemical industry due to its inertness and ability to dissolve a wide range of substances. It is also a starting material in the synthesis of several important organic compounds, including [[pharmaceuticals]] and [[agrochemicals]]. The introduction of a fluorine atom into organic molecules can significantly alter their biological activity, making fluorobenzene a valuable intermediate in medicinal chemistry.&lt;br /&gt;
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==Safety==&lt;br /&gt;
Like many organic solvents, fluorobenzene is flammable and poses health risks if inhaled or ingested. It can cause irritation to the skin, eyes, and respiratory system. Appropriate safety measures, including the use of personal protective equipment and adequate ventilation, are important when handling this compound.&lt;br /&gt;
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[[Category:Organic compounds]]&lt;br /&gt;
[[Category:Fluoroaromatics]]&lt;br /&gt;
{{Chemistry-stub}}&lt;/div&gt;</summary>
		<author><name>Prab</name></author>
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