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alpha,alpha,alpha-Trifluoro-p-tolualdehyde CAS:455-19-6

Short Description:

Catalog Number: XD96237
Cas: 455-19-6
Molecular Formula: C8H5F3O
Molecular Weight: 174.12
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Product Detail

Product Tags

Catalog Number XD96237
Product Name alpha,alpha,alpha-Trifluoro-p-tolualdehyde
CAS 455-19-6
Molecular Formula C8H5F3O
Molecular Weight 174.12
Storage Details Ambient

 

Product Specification

Appearance White powder
Assay 99% min

 

Alpha,alpha,alpha-Trifluoro-p-tolualdehyde, also known as trifluoro-p-tolualdehyde, is a chemical compound with the molecular formula C8H6F3CHO. It has several effects and applications due to its unique chemical structure and properties.One of the primary effects of trifluoro-p-tolualdehyde is its use as a versatile building block in organic synthesis. It contains a trifluoromethyl group (-CF3), which is a highly electron-withdrawing group. This group enhances the reactivity of the compound, allowing it to undergo various transformations. Trifluoro-p-tolualdehyde can be used in the synthesis of pharmaceutical compounds, agrochemicals, and other specialty chemicals. Its reactivity enables the formation of new carbon-carbon and carbon-heteroatom bonds, making it valuable for the creation of complex organic molecules.Moreover, trifluoro-p-tolualdehyde is known for its use in the synthesis of biologically active compounds. The presence of the trifluoromethyl group can impart unique pharmacological properties to these compounds, enhancing their efficacy or specificity. Trifluoro-p-tolualdehyde has been utilized in the production of drugs with applications in various therapeutic areas, including antiviral, antibacterial, antifungal, and anti-inflammatory agents. The trifluoromethyl group can mimic essential functional groups found in natural products or modulate the interaction of the drug with its biological targets, resulting in improved pharmaceutical properties.Additionally, trifluoro-p-tolualdehyde has applications in materials science. It can be used as a building block for the preparation of functionalized polymers and materials with tailored properties. For instance, the trifluoromethyl group can enhance the chemical stability, hydrophobicity, or thermal resistance of polymers. This makes trifluoro-p-tolualdehyde useful in the development of specialty coatings, adhesives, and other advanced materials.Furthermore, trifluoro-p-tolualdehyde has been used as a valuable reagent in analytical chemistry. It can react selectively with certain functional groups or compounds, enabling their detection or quantification. Trifluoro-p-tolualdehyde has been employed in methods such as derivatization reactions for gas chromatography and liquid chromatography analyses. Its reactivity with specific analytes allows for increased sensitivity and selectivity in the determination of target compounds in various samples.In conclusion, trifluoro-p-tolualdehyde exhibits several effects and applications due to its unique chemical structure. It serves as a building block in organic synthesis, enabling the creation of complex molecules in the pharmaceutical and agrochemical industries. Trifluoro-p-tolualdehyde is also utilized in the synthesis of biologically active compounds, providing enhanced pharmacological properties. Its applications extend to materials science, where it contributes to the development of advanced materials. Additionally, trifluoro-p-tolualdehyde finds use in analytical chemistry, allowing for selective reactions and improved detection methods. Overall, trifluoro-p-tolualdehyde plays a crucial role in various fields, contributing to advancements in medicine, materials, and analytical techniques.


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    alpha,alpha,alpha-Trifluoro-p-tolualdehyde CAS:455-19-6