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Catalog Number:
02674
CAS Number:
198561-81-8
Fmoc-N-methyl-O-benzyl-L-threonine
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-N-Me-L-Thr(Bzl)-OH
Documents
$72.31 /1G
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Product Information

Fmoc-N-methyl-O-benzyl-L-threonine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a unique Fmoc (fluorenylmethyloxycarbonyl) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its N-methyl and O-benzyl modifications enhance its stability and solubility, making it an ideal choice for researchers looking to streamline their synthesis processes.

In practical applications, Fmoc-N-methyl-O-benzyl-L-threonine is particularly valuable in the development of therapeutic peptides and biologically active compounds. Its ability to facilitate the formation of complex peptide structures allows for the exploration of novel drug candidates with improved efficacy and reduced side effects. Additionally, this compound's compatibility with various coupling reagents and its ease of deprotection make it a preferred choice among chemists in both academic and industrial settings.

Synonyms
Fmoc-N-Me-L-Thr(Bzl)-OH
CAS Number
198561-81-8
Purity
≥ 98% (HPLC)
Molecular Formula
C27H27NO5
Molecular Weight
445.5
MDL Number
MFCD00235882
PubChem ID
53394983
Melting Point
112 - 120 °C
Appearance
White powder
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-N-Me-L-Thr(Bzl)-OH
CAS Number
198561-81-8
Purity
≥ 98% (HPLC)
Molecular Formula
C27H27NO5
Molecular Weight
445.5
MDL Number
MFCD00235882
PubChem ID
53394983
Melting Point
112 - 120 °C
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

Fmoc-N-methyl-O-benzyl-L-threonine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a crucial building block in the synthesis of peptides, allowing for the introduction of specific amino acid sequences in drug development.
  • Drug Design: Its unique structure enables researchers to create more effective and targeted therapeutic agents, particularly in the field of oncology and neurology.
  • Bioconjugation: The chemical is employed in bioconjugation processes, facilitating the attachment of biomolecules to drugs or imaging agents, enhancing their efficacy and specificity.
  • Research in Protein Engineering: It aids in the modification of proteins, providing insights into protein structure and function, which is essential for developing novel biopharmaceuticals.
  • Analytical Chemistry: The compound is used in various analytical techniques, including chromatography, to separate and identify complex mixtures in biological samples.

Citations