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2-(trifluoromethoxy)fluorobenzene CAS:2106-18-5

Short Description:

Catalog Number: XD96201
Cas: 2106-18-5
Molecular Formula: C7H4F4O
Molecular Weight: 180.1
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Product Detail

Product Tags

Catalog Number XD96201
Product Name 2-(trifluoromethoxy)fluorobenzene
CAS 2106-18-5
Molecular Formula C7H4F4O
Molecular Weight 180.1
Storage Details Ambient

 

Product Specification

Appearance White powder
Assay 99% min

 

2-(Trifluoromethoxy)fluorobenzene is a chemical compound with the molecular formula C7H4F3O. It consists of a fluorobenzene ring (C6H4F) with a trifluoromethoxy group (-OCF3) attached at the 2-position. This compound exhibits various effects and applications due to its unique structural characteristics.One effect of 2-(trifluoromethoxy)fluorobenzene is its ability to act as a strong electron-withdrawing group. The trifluoromethoxy group is highly electronegative, causing it to draw electron density away from the fluorobenzene ring. This electron-withdrawing effect can result in increased reactivity and stability of the compound in various chemical reactions. It can also influence the acidity and basicity of neighboring functional groups, making it useful in organic synthesis and catalysis.Another effect of 2-(trifluoromethoxy)fluorobenzene is its impact on lipophilicity and hydrophobicity. The trifluoromethoxy group imparts hydrophobic properties to the compound, making it soluble in nonpolar solvents and favoring interactions with hydrophobic regions of biological molecules. This characteristic can be advantageous in drug discovery and development, as it allows the compound to penetrate lipid membranes more efficiently. Additionally, the lipophilicity of 2-(trifluoromethoxy)fluorobenzene can impact its bioavailability and distribution in the body.Furthermore, the trifluoromethoxy group in 2-(trifluoromethoxy)fluorobenzene may confer unique properties to materials when incorporated. For example, it can enhance the chemical and thermal stability of polymers, making it useful in the development of high-performance materials like coatings, adhesives, and films. It can also modify the surface properties of materials, altering their wettability and interaction with other substances.In summary, the presence of the trifluoromethoxy group in 2-(trifluoromethoxy)fluorobenzene exerts significant effects on its reactivity, lipophilicity, and material properties. Its electron-withdrawing nature and hydrophobic characteristics make it valuable in various fields, including organic synthesis, drug discovery, and materials science. Continued research on this compound and its derivatives may uncover further applications and advantages in different scientific and technological areas.


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    2-(trifluoromethoxy)fluorobenzene CAS:2106-18-5