Bis(2-oxo-3-oxazolidinyl)phosphinic Chloride: Your Key to Advanced Peptide Synthesis
Discover the unparalleled efficiency of this vital reagent for your most demanding chemical synthesis needs.
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Bis(2-oxo-3-oxazolidinyl)phosphinic Chloride
This compound is a highly effective reagent for the acylation of N-methyl amino acids, providing good yields with low epimerization. It is also an efficient reagent for coupling protected amino monothioacids to iminoamino acid residues to form thiopeptide bonds, making it a cornerstone in advanced peptide synthesis.
- Leverage this efficient coupling reagent for successful peptide synthesis, ensuring high yields and minimal side reactions.
- Explore its utility in amino monothioacid coupling to create specialized peptide structures.
- Utilize this versatile compound as a pharmaceutical intermediate for novel drug development.
- Incorporate its unique phosphinic structure into agrochemical formulations for enhanced pest control and plant growth regulation.
Key Advantages Offered
High Coupling Efficiency
Achieve superior results in your synthesis projects with this reliable peptide coupling reagent low epimerization.
Versatile Reactivity
Benefit from its broad applicability, including effective amino monothioacid coupling for complex molecular architectures.
Broad Application Spectrum
This compound serves as a critical pharmaceutical intermediate synthesis component and finds use in agrochemical and polymer industries.
Key Applications
Peptide Synthesis
As a premier peptide synthesis reagent, it ensures efficient bond formation and structural integrity.
Pharmaceutical Development
Its role as a key pharmaceutical intermediate aids in the creation of new therapeutic agents.
Agrochemical Formulation
Contributes to effective pest control and plant growth with its use in agrochemcial formulation.
Polymer Chemistry
Acts as a valuable polymer crosslinking agent, enhancing material properties and thermal stability.
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