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Pentafluorobenzonitrile CAS:773-82-0

Short Description:

Catalog Number: XD95699
Cas: 773-82-0
Molecular Formula: C7F5N
Molecular Weight: 193.07
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Product Detail

Product Tags

Catalog Number XD95699
Product Name Pentafluorobenzonitrile
CAS 773-82-0
Molecular Formula C7F5N
Molecular Weight 193.07
Storage Details Ambient

 

Product Specification

Appearance White powder
Assay 99% min

 

Pentafluorobenzonitrile (C6F5CN) is a chemical compound that consists of a benzene ring with five fluorine substituents and a cyano group (-CN) attached. It has several notable effects and properties:Electron-Withdrawing Nature: The presence of five fluorine atoms in pentafluorobenzonitrile imparts a strong electron-withdrawing effect. This results in a significant decrease in electron density in the benzene ring and the cyano group, making the compound highly electron-deficient. This property influences its reactivity and behavior in various chemical reactions.Increased Acidity: The electron-withdrawing nature of pentafluorobenzonitrile enhances the acidity of the compound compared to benzonitrile. The cyano group's acidic hydrogen is more readily donated due to the electron deficiency induced by the fluorine atoms. This increased acidity can affect reactions involving bases and nucleophiles, as well as acid-base equilibria.Altered Reactivity: The electron-withdrawing effect of pentafluorobenzonitrile impacts its reactivity in numerous chemical transformations. It can influence reaction rates, regioselectivity, and even the type of products obtained. For instance, in nucleophilic addition reactions, the cyano group could attract nucleophiles to the carbon atom, leading to different reaction pathways compared to benzonitrile.Stability: Pentafluorobenzonitrile is known for its stability due to the strong electron-withdrawing effect of the fluorine atoms. This makes it resistant to degradation and decomposition under various conditions. Its stability allows for its use as a starting material in synthetic chemistry.Applications: Pentafluorobenzonitrile finds applications in various fields. Its enhanced acidity and altered reactivity make it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Its electron-deficient nature can also serve as a directing group in organic synthesis, assisting in controlling regioselectivity during reactions.Safety Considerations: While pentafluorobenzonitrile is generally considered safe to handle and use, appropriate safety precautions should be taken. It is advisable to work in a well-ventilated area, wear appropriate protective equipment, and store and handle the compound according to proper protocols.In conclusion, pentafluorobenzonitrile's electron-withdrawing nature, increased acidity, altered reactivity, and stability make it a useful compound in synthetic chemistry. Its applications span various industries, allowing for the development of new compounds and materials. However, safety precautions should always be followed when working with this compound.


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    Pentafluorobenzonitrile CAS:773-82-0