N,N'-Di-tert-butoxycarbonyl-L-histidine: Precision in Peptide Synthesis
Your essential building block for advanced peptide synthesis and complex organic chemistry applications.
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N,N'-Di-tert-butoxycarbonyl-L-histidine
N,N'-Di-tert-butoxycarbonyl-L-histidine (CAS 20866-46-0) is a premium chemical intermediate, primarily recognized for its role in advanced peptide synthesis. Its unique structure, featuring two tert-butoxycarbonyl (Boc) protecting groups on the histidine molecule, provides chemists with superior control over reactions. This makes it an indispensable component for researchers aiming for precise molecular construction in medicinal chemistry and drug development.
- Enhance your peptide synthesis strategy by utilizing this key Boc-protected histidine derivative.
- Leverage CAS 20866-46-0 as a high-purity chemical for demanding organic synthesis projects.
- Discover the benefits of histidine building blocks in creating complex organic molecules for research.
- Understand the applications of Boc-His(Boc)-OH in achieving controlled amino acid protection during synthesis.
Key Advantages
Controlled Reactivity
The dual Boc protection on N,N'-Di-tert-butoxycarbonyl-L-histidine ensures that reactivity is precisely managed, offering a significant advantage in multi-step organic synthesis and peptide assembly.
Versatile Application
As a crucial histidine building block, this compound is vital for researchers involved in medicinal chemistry and pharmaceutical intermediate development, enabling the synthesis of novel therapeutic agents.
Reliable Purity
With a typical purity of ≥98.0%, this compound guarantees consistent and reproducible results in your sensitive chemical reactions, supporting your research integrity.
Key Applications
Peptide Synthesis
This N,N'-Di-tert-butoxycarbonyl-L-histidine is fundamental for solid-phase and solution-phase peptide synthesis, where precise protection of amino and imidazole groups is critical.
Organic Synthesis
Its utility extends to various organic chemistry transformations, serving as a versatile building block for constructing complex molecules and functionalized intermediates.
Medicinal Chemistry
Researchers in medicinal chemistry utilize this compound for the development of new drug candidates, leveraging the imidazole side chain of histidine.
Biochemical Research
It plays a role in biochemical research, particularly in studies involving modified peptides or proteins where protected amino acids are required.
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