Nitrocyclohexane: Difference between revisions

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'''Nitrocyclohexane''' is an [[organic compound]] with the [[chemical formula]] C<sub>6</sub>H<sub>11</sub>NO<sub>2</sub>. It is a [[nitro compound]] and a [[cyclohexane derivative]]. Nitrocyclohexane is a colorless liquid at room temperature and has a strong, unpleasant odor.
{{DISPLAYTITLE:Nitrocyclohexane}}


== Properties ==
== Nitrocyclohexane ==
[[File:Nitrocyclohexane.svg|thumb|right|Structural formula of Nitrocyclohexane]]


Nitrocyclohexane is a colorless liquid with a strong, unpleasant odor. It has a [[molecular weight]] of 129.16 g/mol. The compound is relatively stable under normal conditions, but it can react with strong oxidizing agents, causing a violent reaction.
'''Nitrocyclohexane''' is an organic compound with the chemical formula C_H__NO_. It is a nitroalkane derivative of [[cyclohexane]], where one hydrogen atom is replaced by a nitro group (-NO_). This compound is of interest in various chemical research and industrial applications due to its unique properties.


== Synthesis ==
== Structure and Properties ==
Nitrocyclohexane consists of a six-membered carbon ring, typical of [[cyclohexane]], with a nitro group attached to one of the carbon atoms. The presence of the nitro group significantly alters the chemical properties of the molecule compared to its parent hydrocarbon.


Nitrocyclohexane can be synthesized by the nitration of cyclohexane. This process involves the reaction of cyclohexane with nitric acid in the presence of sulfuric acid as a catalyst. The reaction produces nitrocyclohexane and water as byproducts.
The nitro group is electron-withdrawing, which affects the reactivity of the compound. Nitrocyclohexane is a colorless liquid at room temperature and has a characteristic odor. It is relatively stable but can undergo reactions typical of nitro compounds, such as reduction and nitration.


== Uses ==
== Synthesis ==
Nitrocyclohexane can be synthesized through the nitration of cyclohexane. This process involves the reaction of cyclohexane with a nitrating agent, such as nitric acid, under controlled conditions to introduce the nitro group into the cyclohexane ring.


Nitrocyclohexane is primarily used in the production of other chemicals. It is a precursor to aminocyclohexane, which is used in the synthesis of pharmaceuticals and other organic compounds.
== Applications ==
Nitrocyclohexane is used in organic synthesis as an intermediate. It can be further transformed into various other chemical compounds, making it valuable in the production of pharmaceuticals, agrochemicals, and other industrial chemicals.


== Safety ==
== Safety and Handling ==
As with many nitro compounds, nitrocyclohexane should be handled with care. It is flammable and can pose health risks if inhaled or ingested. Proper safety measures, including the use of personal protective equipment and adequate ventilation, should be employed when working with this chemical.


Nitrocyclohexane is a flammable liquid and can cause burns and eye damage. It should be handled with care and stored in a cool, well-ventilated area away from heat sources and open flames.
== Related Compounds ==
 
* [[Cyclohexane]]
== See also ==
* [[Nitroalkane]]
* [[Nitrobenzene]]


* [[Cyclohexane]]
== See Also ==
* [[Nitration]]
* [[Organic chemistry]]
* [[Organic compound]]
* [[Chemical synthesis]]
* [[Chemical formula]]


[[Category:Organic compounds]]
[[Category:Nitro compounds]]
[[Category:Nitro compounds]]
[[Category:Cyclohexanes]]
[[Category:Organic chemistry]]
 
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Latest revision as of 11:05, 15 February 2025


Nitrocyclohexane[edit]

Structural formula of Nitrocyclohexane

Nitrocyclohexane is an organic compound with the chemical formula C_H__NO_. It is a nitroalkane derivative of cyclohexane, where one hydrogen atom is replaced by a nitro group (-NO_). This compound is of interest in various chemical research and industrial applications due to its unique properties.

Structure and Properties[edit]

Nitrocyclohexane consists of a six-membered carbon ring, typical of cyclohexane, with a nitro group attached to one of the carbon atoms. The presence of the nitro group significantly alters the chemical properties of the molecule compared to its parent hydrocarbon.

The nitro group is electron-withdrawing, which affects the reactivity of the compound. Nitrocyclohexane is a colorless liquid at room temperature and has a characteristic odor. It is relatively stable but can undergo reactions typical of nitro compounds, such as reduction and nitration.

Synthesis[edit]

Nitrocyclohexane can be synthesized through the nitration of cyclohexane. This process involves the reaction of cyclohexane with a nitrating agent, such as nitric acid, under controlled conditions to introduce the nitro group into the cyclohexane ring.

Applications[edit]

Nitrocyclohexane is used in organic synthesis as an intermediate. It can be further transformed into various other chemical compounds, making it valuable in the production of pharmaceuticals, agrochemicals, and other industrial chemicals.

Safety and Handling[edit]

As with many nitro compounds, nitrocyclohexane should be handled with care. It is flammable and can pose health risks if inhaled or ingested. Proper safety measures, including the use of personal protective equipment and adequate ventilation, should be employed when working with this chemical.

Related Compounds[edit]

See Also[edit]