Propargyl-PEG2-OH: A Versatile PEG-Based Linker for Advanced Chemical Synthesis
Unlock innovative synthesis pathways with our high-purity PEG-based linker, essential for PROTAC and click chemistry applications.
Get a Quote & SampleProduct Core Value
Propargyl-PEG2-OH
Propargyl-PEG2-OH stands as a crucial PEG-based linker, specifically engineered for the efficient synthesis of complex molecules like Thalidomide-O-PEG2-propargyl. Its chemical structure, C7H12O3, and a molecular weight of 144.16800, along with a purity of 99.2%, underscore its reliability for demanding research and development projects. This versatile compound is instrumental in advancing fields such as targeted protein degradation through PROTAC technology and facilitates novel molecular construction via click chemistry.
- Leverage the power of click chemistry to build intricate molecules, making the synthesis of Thalidomide-O-PEG2-propargyl a streamlined process.
- Achieve superior experimental outcomes with a highly pure reagent, boasting a purity level of 99.2%, ensuring consistent and reliable results.
- Explore advanced drug discovery avenues by utilizing Propargyl-PEG2-OH as a key component in PROTAC linker strategies.
- Benefit from the well-defined chemical properties, including a molecular weight of 144.16800 and a density of 1.044g/cm3, for precise formulation and application.
Key Advantages of Propargyl-PEG2-OH
Enhanced Synthesis Efficiency
The unique structure of Propargyl-PEG2-OH facilitates efficient chemical synthesis, particularly in the development of PROTACs, streamlining complex molecular assembly.
High Purity and Reliability
With a purity of 99.2%, this linker ensures the integrity of your synthesized compounds, minimizing side reactions and maximizing yield in critical research.
Versatile Application in Drug Discovery
Its role as a PEG-based linker makes it invaluable for creating bispecific molecules for protein degradation, directly supporting cutting-edge drug discovery efforts.
Key Applications
PROTAC Synthesis
Propargyl-PEG2-OH is an essential building block for synthesizing PROTACs, enabling targeted protein degradation strategies in pharmaceutical research.
Click Chemistry
Its terminal alkyne group makes it an ideal reagent for click chemistry reactions, allowing for efficient conjugation and molecular assembly.
Thalidomide Conjugate Synthesis
This linker is specifically utilized in the synthesis of Thalidomide-O-PEG2-propargyl, a critical component in certain pharmaceutical development pathways.
Advanced Chemical Linker Design
Researchers can leverage this linker in the design of new chemical entities, exploring novel applications in medicinal chemistry and materials science.