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Catalog Number:
02672
CAS Number:
84000-14-6
Fmoc-N-methyl-O-benzyl-L-serine
Purity:
99+%
Synonym(s):
Fmoc-N-Me-L-Ser(Bzl)-OH
Documents
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Product Information

Fmoc-N-methyl-O-benzyl-L-serine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc (fluorenylmethyloxycarbonyl) group, which allows for selective deprotection during the synthesis of peptides, making it an essential building block for researchers in the fields of medicinal chemistry and biochemistry. Its unique structure, which includes a methyl and benzyl group, enhances its stability and solubility, facilitating smoother reactions and improved yields in complex peptide sequences.

In practical applications, Fmoc-N-methyl-O-benzyl-L-serine is particularly valuable in the development of peptide-based therapeutics, where precise amino acid sequences are crucial for biological activity. Its ability to provide a stable and functional side chain makes it an excellent choice for synthesizing peptides with specific pharmacological properties. Researchers appreciate its compatibility with various coupling reagents and its effectiveness in solid-phase peptide synthesis, which streamlines the production of high-purity peptides for further study or therapeutic use.

Synonyms
Fmoc-N-Me-L-Ser(Bzl)-OH
CAS Number
84000-14-6
Purity
99+%
Molecular Formula
C26H25NO5
Molecular Weight
431.5
MDL Number
MFCD00235880
PubChem ID
53395243
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-N-Me-L-Ser(Bzl)-OH
CAS Number
84000-14-6
Purity
99+%
Molecular Formula
C26H25NO5
Molecular Weight
431.5
MDL Number
MFCD00235880
PubChem ID
53395243
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-serine is widely utilized in research focused on:

  • Peptide Synthesis: This compound is commonly used as a building block in solid-phase peptide synthesis, allowing researchers to create complex peptides with specific sequences efficiently.
  • Drug Development: Its unique structure makes it valuable in the design of novel pharmaceuticals, particularly in developing targeted therapies that require precise amino acid configurations.
  • Bioconjugation: The benzyl group in this compound facilitates bioconjugation processes, enabling the attachment of drugs or imaging agents to biomolecules, which is crucial in targeted drug delivery systems.
  • Protein Engineering: Researchers utilize this compound to modify proteins, enhancing their stability and functionality, which is essential in developing biocatalysts and therapeutic proteins.
  • Research in Neuroscience: Its properties make it suitable for studying neurotransmitter interactions, aiding in the development of treatments for neurological disorders.

Citations