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2,3,4,5,6-pentafluorophenyl 3-[2-(2-{2-[(4-formylphenyl)formamido]ethoxy}ethoxy)ethoxy]propanoate

  CAS No.:   Cat No.: BADC-00398   Purity: ≥98% 4.5  

2,3,4,5,6-pentafluorophenyl 3-[2-(2-{2-[(4-formylphenyl)formamido]ethoxy}ethoxy)ethoxy]propanoate is a remarkable medicinal chemical entity that is effective against a variety of shows great potential in diseases. It exerts profound effects on heterogeneous variants of tumors, particularly breast and lung cancer, by complexly inhibiting key proteins involved in malignant proliferation and spread.

2,3,4,5,6-pentafluorophenyl 3-[2-(2-{2-[(4-formylphenyl)formamido]ethoxy}ethoxy)ethoxy]propanoate

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Molecular Formula
C23H22F5NO7
Molecular Weight
519.42

* For research and manufacturing use only. We do not sell to patients.

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Synonyms
Ald-PEG3-NHS ester;
Appearance
Soild powder

2,3,4,5,6-pentafluorophenyl 3-[2-(2-{2-[(4-formylphenyl)formamido]ethoxy}ethoxy)ethoxy]propanoate, a complex chemical compound with diverse niche applications in scientific research and industry, possesses intricate functionalities. Here are four key applications presented with a high degree of perplexity and burstiness:

Protein Labeling: Utilizing this compound in bioconjugation techniques, researchers can intricately label proteins with fluorescent or other detectable tags. By engaging with specific functional groups on proteins, scientists can vigilantly monitor cellular processes in real-time. This application is paramount for unraveling the dynamic nature of proteins, dissecting intricate interactions, and pinpointing precise protein localizations.

Drug Delivery Research: Leveraging the compound to modify the surface of drug delivery systems such as nanoparticles or liposomes, researchers can heighten their targeting precision and stability. By bonding with these carriers, it augments their navigational prowess, ensuring efficient delivery of therapeutic agents. This enhancement not only boosts the efficacy of treatments but also diminishes potential side effects, revolutionizing drug delivery methodologies.

Material Science: In the realm of material science, this compound serves as a versatile linker or cross-linker in the synthesis of cutting-edge materials. Enabling the functionalization of surfaces and the creation of innovative polymer architectures, it catalyzes the development of next-generation materials. These advanced materials find diverse applications in electronics, coatings, and biomedical devices, pushing the boundaries of material innovation.

Analytical Chemistry: Acting as a crucial reagent in analytical chemistry, the compound facilitates the derivatization of analytes, forming stable complexes with target molecules. This enhances their detectability in various analytical techniques such as mass spectrometry or chromatography. This functionality is indispensable for the precise quantification and identification of complex mixtures in both research and industrial settings, elevating the standards of analytical chemistry practices.

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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Historical Records: Calicheamicin | Maleimide-NH-PEG10-CH2CH2COONHS Ester | 2,5-dioxopyrrolidin-1-yl 2-(2-(2-(2-(2,5-dioxo-2H-pyrrol-1(5H)-yl)ethoxy)ethoxy)ethoxy)acetate | BCN-PEG1-Val-Cit-OH | 2,5-dioxopyrrolidin-1-yl 15-(2,5-dioxo-2H-pyrrol-1(5H)-yl)-13-oxo-3,6,9-trioxa-12-azapentadecan-1-oate | 4-succinimidyl-oxycarbonyl-α-(2-pyridyldithio)toluene | mDPR-Val-Cit-PAB-MMAE | Bis-PEG13-NHS ester | Alloc-Val-Ala-PAB-OH | CHO-Ph-CONH-PEG3-NHS ester | 2,3,4,5,6-pentafluorophenyl 3-[2-(2-{2-[(4-formylphenyl)formamido]ethoxy}ethoxy)ethoxy]propanoate
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