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4-(Trifluoromethoxy)nitrobenzene CAS:713-65-5

Short Description:

Catalog Number: XD96202
Cas: 713-65-5
Molecular Formula: C7H4F3NO3
Molecular Weight: 207.11
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Product Detail

Product Tags

Catalog Number XD96202
Product Name 4-(Trifluoromethoxy)nitrobenzene
CAS 713-65-5
Molecular Formula C7H4F3NO3
Molecular Weight 207.11
Storage Details Ambient

 

Product Specification

Appearance White powder
Assay 99% min

 

4-(Trifluoromethoxy)nitrobenzene is a chemical compound with the molecular formula C7H4F3NO2. It is composed of a nitrobenzene ring (C6H4NO2) with a trifluoromethoxy group (-OCF3) attached at the 4-position. This unique structural arrangement imparts several notable effects and applications to this compound.One effect of 4-(Trifluoromethoxy)nitrobenzene is its electron-withdrawing capability. The trifluoromethoxy group is highly electronegative, enhancing the electron-withdrawing nature of the nitro group (-NO2) present in the molecule. This electron-withdrawing effect makes 4-(Trifluoromethoxy)nitrobenzene a strong electron acceptor, allowing it to participate in various types of chemical reactions, such as nucleophilic substitutions and electrophilic aromatic substitutions. Additionally, this compound can act as a ligand in coordination chemistry due to its ability to form stable complexes with metal ions.Another effect of 4-(Trifluoromethoxy)nitrobenzene is its influence on lipophilicity and hydrophobicity. The trifluoromethoxy group enhances the hydrophobic character of the compound, making it more soluble in nonpolar solvents and favoring interaction with hydrophobic regions of biological molecules. This property can be advantageous in drug discovery and development, potentially improving the compound's ability to permeate lipid membranes and increasing its bioavailability.Furthermore, the presence of the trifluoromethoxy group in 4-(Trifluoromethoxy)nitrobenzene may confer unique properties to materials when incorporated. For instance, it can enhance the chemical and thermal stability of polymers, making it useful in the production of high-performance materials like coatings, adhesives, and films. Additionally, the lipophilicity of this compound can impact its behavior as a surfactant or emulsifier, allowing it to modify surface properties of materials, alter wettability, and facilitate dispersion of immiscible substances.In summary, 4-(Trifluoromethoxy)nitrobenzene exhibits electron-withdrawing characteristics, influencing its reactivity and ability to form coordination complexes. It also possesses lipophilic and hydrophobic properties, which can impact its solubility, bioavailability, and interaction with biological systems. Furthermore, it has the potential to enhance the stability and surface properties of materials when incorporated. The distinctive features of 4-(Trifluoromethoxy)nitrobenzene make it an intriguing compound with applications in organic synthesis, drug discovery, coordination chemistry, and materials science. Further exploration and research into this compound may reveal additional effects and potential applications.


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    4-(Trifluoromethoxy)nitrobenzene CAS:713-65-5