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4-(Trifluoromethoxy)phenylisocyanate CAS:352-67-0

Short Description:

Catalog Number: XD96199
Cas: 352-67-0
Molecular Formula: C7H4F4O
Molecular Weight: 180.1
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Product Detail

Product Tags

Catalog Number XD96199
Product Name 4-(Trifluoromethoxy)phenylisocyanate
CAS 352-67-0
Molecular Formula C7H4F4O
Molecular Weight 180.1
Storage Details Ambient

 

Product Specification

Appearance White powder
Assay 99% min

 

4-(Trifluoromethoxy)phenylisocyanate is a chemical compound with the formula C8H4F3NO2. It consists of a phenyl group (C6H5) attached to an isocyanate group (-NCO), with a trifluoromethoxy group (-OCF3) substituting on the phenyl ring. This compound exhibits interesting effects and applications in various areas.One prominent effect of 4-(trifluoromethoxy)phenylisocyanate is its reactivity towards nucleophiles. The isocyanate group readily reacts with nucleophilic entities such as amines, alcohols, and thiols, forming corresponding ureas, carbamates, and thiocarbamates, respectively. These reactions are widely utilized in synthetic organic chemistry for the synthesis of diverse compounds. For example, the compound can be employed as a building block in the preparation of pharmaceutical agents, agrochemicals, or materials with desired properties.The trifluoromethoxy group in 4-(trifluoromethoxy)phenylisocyanate not only enhances the compound's reactivity but also influences its physicochemical properties. The presence of this electron-withdrawing group alters the electron density and polarity of the phenyl ring, making it attractive for applications where electronic effects are crucial, such as in the design of organic dyes, catalysts, or fluorescent probes. Additionally, the trifluoromethoxy group imparts enhanced lipophilicity and metabolic stability to the compound, potentially improving its bioavailability and pharmacokinetic properties in pharmaceutical research.Furthermore, 4-(trifluoromethoxy)phenylisocyanate can participate in various organic reactions, including cycloaddition reactions, rearrangements, and cross-coupling reactions. These transformations can lead to the synthesis of complex molecules with diverse structures and functionalities.In materials science, this compound can be employed as a reactive intermediate for the preparation of functional materials or surface modifications. The isocyanate group can react with a wide range of functional groups, allowing for the attachment of desired functionalities onto surfaces or polymers. This feature finds applications in coatings, adhesives, or controlled drug release systems, where tailored properties are desired.Overall, 4-(trifluoromethoxy)phenylisocyanate exhibits versatile reactivity and properties that make it valuable in various fields. Its ability to react with nucleophiles and participate in diverse organic transformations opens up possibilities in synthetic chemistry, pharmaceutical research, and materials science. As researchers continue to explore the compound's unique features, its applications are likely to expand further.


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    4-(Trifluoromethoxy)phenylisocyanate CAS:352-67-0