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2-(Trifluoromethoxy)chlorobenzene CAS:450-96-4

Short Description:

Catalog Number: XD96198
Cas: 450-96-4
Molecular Formula: C7H4ClF3O
Molecular Weight: 196.55
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Product Detail

Product Tags

Catalog Number XD96198
Product Name 2-(Trifluoromethoxy)chlorobenzene
CAS 450-96-4
Molecular Formula C7H4ClF3O
Molecular Weight 196.55
Storage Details Ambient

 

Product Specification

Appearance White powder
Assay 99% min

 

2-(Trifluoromethoxy)chlorobenzene is a chemical compound with the formula C7H4ClF3O. It consists of a chloro group (-Cl) and a trifluoromethoxy group (-OCF3) attached to a benzene ring. This compound has several effects and applications in various fields.One important effect of 2-(trifluoromethoxy)chlorobenzene is its ability to act as an efficient solvent and reagent in organic synthesis. Its trifluoromethoxy group is highly electron-withdrawing, making it an excellent leaving group in substitution reactions. This property allows for the synthesis of various important compounds, including pharmaceuticals, agrochemicals, and materials with desirable properties. Additionally, the chloro group can undergo nucleophilic substitution reactions, further expanding the compound's synthetic utility.In pharmaceutical research and development, 2-(trifluoromethoxy)chlorobenzene is particularly interesting due to the presence of the trifluoromethoxy group. This group enhances the lipophilicity and metabolic stability of the compound, leading to improved drug absorption, distribution, and bioavailability. It also influences the compound's binding affinity to target proteins, potentially increasing its potency and efficacy. Consequently, the compound finds applications in the synthesis of drug candidates or as a starting material for the modification of existing drugs to improve their pharmacological properties.The trifluoromethoxy group in 2-(trifluoromethoxy)chlorobenzene also imparts unique physicochemical properties to the compound. It significantly increases the compound's electron density and enhances its ability to form intermolecular interactions, such as halogen bonding or π-π stacking. These properties can be exploited in the development of catalysts, dyes, or fluorescent probes, among other applications.Furthermore, the trifluoromethoxy group is responsible for the compound's exceptional thermal and chemical stability. This stability allows for its utilization in applications involving harsh reaction conditions or elevated temperatures, such as polymer synthesis or materials science.In summary, 2-(trifluoromethoxy)chlorobenzene demonstrates versatile effects and applications in various fields. Its utility as a solvent and reagent in organic synthesis, especially in pharmaceutical research, is highly valuable. The trifluoromethoxy group enhances the compound's lipophilicity, stability, and reactivity, making it useful in drug discovery, catalyst development, and materials science. As researchers continue to explore the compound's unique properties, its applications in these fields are likely to expand.


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    2-(Trifluoromethoxy)chlorobenzene CAS:450-96-4