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2-bromoethyl(diphenyl)sulfanium,trifluoromethanesulfonate CAS:247129-85-7

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Catalog Number: XD96369
Cas: 247129-85-7
Molecular Formula: C15H14BrF3O3S2
Molecular Weight: 443.2990696
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Product Tags

Catalog Number XD96369
Product Name 2-bromoethyl(diphenyl)sulfanium,trifluoromethanesulfonate
CAS 247129-85-7
Molecular Formula C15H14BrF3O3S2
Molecular Weight 443.2990696
Storage Details Ambient

 

Product Specification

Appearance White powder
Assay 99% min

 

2-bromoethyl(diphenyl)sulfanium, trifluoromethanesulfonate is a chemical compound that consists of a bromoethyl group attached to a diphenylsulfanium cation, which is then bonded to a trifluoromethanesulfonate anion. This complex compound can have several effects and applications.One significant effect of 2-bromoethyl(diphenyl)sulfanium, trifluoromethanesulfonate is its ability to act as a powerful alkylating agent. Alkylation refers to the transfer of an alkyl group to a nucleophile, and this compound is widely used in organic synthesis to introduce alkyl groups into various molecules. The bromoethyl group in this compound is highly reactive, allowing it to react with a wide range of substrates and facilitate the synthesis of complex organic compounds.Moreover, 2-bromoethyl(diphenyl)sulfanium, trifluoromethanesulfonate can be employed as a precursor in the synthesis of pharmaceuticals and bioactive compounds. Its alkylating properties make it useful in the modification of drug molecules, leading to the development of new medications with enhanced properties or improved effectiveness. This compound serves as a valuable building block in medicinal chemistry, enabling the creation of diverse drug candidates.Additionally, this compound may find applications in chemical research and laboratory settings. It can be used for the protection of hydroxyl or amine functional groups during chemical reactions. By temporarily attaching the diphenylsulfonium group to these reactive sites, undesired reactions can be avoided, ensuring selective reactions and yielding desired products. Subsequently, the protection group can be removed under appropriate conditions, revealing the original functional group.Furthermore, 2-bromoethyl(diphenyl)sulfanium, trifluoromethanesulfonate can act as a catalyst in certain chemical transformations. It can facilitate various reactions by providing a favorable environment for reactants to come together and undergo a reaction. Its strong electron-withdrawing trifluoromethanesulfonate anion enhances its catalytic activity, allowing for the synthesis of complex molecules and increasing reaction efficiency.However, it is essential to note that this compound should be handled with caution due to its potential health hazards. It can cause irritation to the skin, eyes, and respiratory system if proper safety precautions are not taken. Adequate protective measures, such as wearing gloves, goggles, and working in a well-ventilated area, should be followed when using this compound.In conclusion, 2-bromoethyl(diphenyl)sulfanium, trifluoromethanesulfonate serves as a versatile compound with various effects and applications. Its alkylating properties make it valuable in organic synthesis and pharmaceutical research, allowing for the modification and development of new drug molecules. Additionally, it can be used as a protective group in chemical reactions and as a catalyst in various transformations. Nonetheless, it is crucial to handle this compound safely to prevent any adverse health effects.


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    2-bromoethyl(diphenyl)sulfanium,trifluoromethanesulfonate CAS:247129-85-7