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Catalog Number:
35202
CAS Number:
704910-17-8
Fmoc-allyl-L-serine
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-L-Ser(allyl)-OH
Documents
$130.00 /100MG
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Product Information

Fmoc-allyl-L-serine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its unique allyl side chain enhances its reactivity, making it an excellent choice for applications in organic synthesis and medicinal chemistry. Researchers appreciate its stability under various conditions, which allows for streamlined synthesis processes and improved yields in peptide formation.

In addition to its role in peptide synthesis, Fmoc-allyl-L-serine is also valuable in the development of bioactive compounds and pharmaceuticals. Its structural properties enable the incorporation of functional groups that can lead to the creation of novel therapeutic agents. This compound is particularly beneficial in the fields of biochemistry and molecular biology, where it aids in the design of peptides with specific biological activities. With its robust applications and favorable characteristics, Fmoc-allyl-L-serine stands out as a crucial tool for researchers and industry professionals alike.

Synonyms
Fmoc-L-Ser(allyl)-OH
CAS Number
704910-17-8
Purity
≥ 98% (HPLC)
Molecular Formula
C21H21NO5
Molecular Weight
367.41
MDL Number
MFCD03094795
PubChem ID
76667569
Appearance
White powder or solid
Optical Rotation
[a]D20
Conditions
Store at ≤ -20 °C
General Information
Synonyms
Fmoc-L-Ser(allyl)-OH
CAS Number
704910-17-8
Purity
≥ 98% (HPLC)
Molecular Formula
C21H21NO5
Molecular Weight
367.41
MDL Number
MFCD03094795
PubChem ID
76667569
Appearance
White powder or solid
Optical Rotation
[a]D20
Conditions
Store at ≤ -20 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-allyl-L-serine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis (SPPS). Its Fmoc protecting group allows for easy deprotection, facilitating the assembly of complex peptide sequences.
  • Drug Development: In pharmaceutical research, Fmoc-allyl-L-serine can be used to create peptide-based drugs. Its unique structure can enhance the bioactivity of therapeutic peptides, making it valuable in drug formulation.
  • Bioconjugation: The allyl group in this compound allows for selective bioconjugation reactions, enabling researchers to attach various biomolecules to peptides. This application is essential in developing targeted therapies and diagnostics.
  • Protein Engineering: This chemical is useful in modifying proteins to improve their stability and function. By incorporating Fmoc-allyl-L-serine into proteins, researchers can enhance their properties for various applications, including enzyme catalysis and antibody development.
  • Research in Chemical Biology: It plays a significant role in studying protein interactions and functions. By utilizing this compound, researchers can explore the effects of specific amino acid modifications on protein behavior, aiding in the understanding of biological processes.

Citations