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Catalog Number:
05520
CAS Number:
201217-86-9
Boc-O-tert-butyl-D-threonine
Purity:
≥ 98% (HPLC)
Synonym(s):
Boc-D-Thr(tBu)-OH
Documents
$113.87 /1G
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Product Information

Boc-O-tert-butyl-D-threonine is a versatile amino acid derivative widely utilized in peptide synthesis and pharmaceutical research. This compound features a tert-butoxycarbonyl (Boc) protecting group, which enhances its stability and solubility, making it an ideal choice for researchers focused on developing complex peptides and biologically active compounds. Its unique structure allows for selective reactions, facilitating the synthesis of peptides with specific functionalities, which is crucial in drug development and biochemistry.

In addition to its role in peptide synthesis, Boc-O-tert-butyl-D-threonine is also valuable in the production of various bioactive molecules and can serve as a building block in the design of therapeutic agents. Its ability to provide steric hindrance while maintaining reactivity makes it a preferred choice for chemists looking to optimize reaction conditions and yields. Researchers in the fields of medicinal chemistry and biochemistry will find this compound essential for advancing their projects and achieving desired outcomes in peptide-based therapies.

Synonyms
Boc-D-Thr(tBu)-OH
CAS Number
201217-86-9
Purity
≥ 98% (HPLC)
Molecular Formula
C13H25NO5
Molecular Weight
275.3
MDL Number
MFCD00236876
PubChem ID
499095
Appearance
White powder
Conditions
Store at 0-8°C
General Information
Synonyms
Boc-D-Thr(tBu)-OH
CAS Number
201217-86-9
Purity
≥ 98% (HPLC)
Molecular Formula
C13H25NO5
Molecular Weight
275.3
MDL Number
MFCD00236876
PubChem ID
499095
Appearance
White powder
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-O-tert-butyl-D-threonine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for the selective modification of amino acids without affecting others. This is particularly useful in the pharmaceutical industry for developing new drugs.
  • Bioconjugation: It plays a crucial role in bioconjugation processes, where it helps in attaching biomolecules to surfaces or other molecules, enhancing the effectiveness of diagnostic tools and therapeutic agents.
  • Protein Engineering: Researchers use it to modify proteins for better stability and functionality, which is essential in biotechnology applications, including enzyme production and vaccine development.
  • Drug Development: The compound is involved in the design of novel therapeutic agents, particularly in the development of amino acid derivatives that can target specific biological pathways.
  • Research in Chiral Chemistry: Its chiral properties make it valuable in studies focused on asymmetric synthesis, helping chemists create more efficient and selective reactions compared to non-chiral counterparts.

Citations