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3-Trifluoromethylbenzaldehyde CAS:454-89-7

Short Description:

Catalog Number: XD96239
Cas: 454-89-7
Molecular Formula: C8H5F3O
Molecular Weight: 174.12
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Product Detail

Product Tags

Catalog Number XD96239
Product Name 3-Trifluoromethylbenzaldehyde
CAS 454-89-7
Molecular Formula C8H5F3O
Molecular Weight 174.12
Storage Details Ambient

 

Product Specification

Appearance White powder
Assay 99% min

 

3-Trifluoromethylbenzaldehyde, also known as 3-CF3C6H4CHO, is a chemical compound that exhibits several effects and applications due to its unique structure and properties.One of the primary effects of 3-Trifluoromethylbenzaldehyde is its electron-withdrawing capability. The trifluoromethyl group (-CF3) attached to the benzaldehyde moiety is highly electron-withdrawing, which enhances the reactivity of the compound. This property makes it a useful building block in organic synthesis. It can undergo various reactions, such as nucleophilic addition reactions, condensation reactions, and transformation into other functional groups. These reactions allow for the creation of complex organic molecules, making 3-Trifluoromethylbenzaldehyde a versatile compound in synthetic chemistry.In addition to its role in organic synthesis, 3-Trifluoromethylbenzaldehyde has applications in the field of pharmaceuticals. The CF3 group enhances the lipophilicity and metabolic stability of the compound, which can impact its biological activity. This compound has been utilized in the synthesis of biologically active compounds, particularly in drug discovery. The trifluoromethyl group can improve the activity and specificity of the resulting molecules, making 3-Trifluoromethylbenzaldehyde derivatives valuable in the development of drugs with applications in various therapeutic areas, such as anti-inflammatory, antiviral, and anticancer agents.Furthermore, 3-Trifluoromethylbenzaldehyde can also be used as a precursor in the synthesis of specialty chemicals and materials. The trifluoromethyl group imparts unique properties to the resulting compounds, such as improved thermal stability, chemical resistance, or hydrophobicity. These properties make 3-Trifluoromethylbenzaldehyde derivatives useful in the development of specialty coatings, plastics, and other materials with specific applications.Additionally, 3-Trifluoromethylbenzaldehyde has applications in chemical research as a reagent or intermediate in various reactions. It can participate in selective reactions with specific functional groups or compounds, enabling their detection or modification. This property has applications in analytical chemistry, where 3-Trifluoromethylbenzaldehyde derivatives can be used as derivatizing agents for gas chromatography or liquid chromatography analyses. These derivatives can enhance the detectability, sensitivity, and selectivity of the analyzed compounds.In conclusion, 3-Trifluoromethylbenzaldehyde possesses unique properties that make it valuable in various fields. Its electron-withdrawing capability and reactivity make it a versatile compound in organic synthesis. It has applications in pharmaceutical research, where it enhances the activity and specificity of drugs. Furthermore, it has applications in the development of specialty chemicals and materials with unique properties. Finally, its reactivity and selectivity find applications in analytical chemistry. Overall, 3-Trifluoromethylbenzaldehyde is a valuable compound with a wide range of effects and applications.


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    3-Trifluoromethylbenzaldehyde CAS:454-89-7