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Catalog Number:
11433
CAS Number:
252206-27-2
Fmoc-(2R,3S-3-phenylisoserine
Purity:
≥ 99% (HPLC)
Synonym(s):
(2R,3S-3-(Fmoc-amino)-2-hydroxy-3-phenyl-propanoic acid
Documents
$166.95 /100MG
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Product Information

Fmoc-(2R,3S)-3-phenylisoserine 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 complex peptides. Its unique structure, characterized by the presence of a phenyl group, enhances its stability and solubility, making it an ideal choice for researchers and professionals in the pharmaceutical and biotechnology industries.

The practical applications of Fmoc-(2R,3S)-3-phenylisoserine extend to the development of bioactive peptides and therapeutic agents. It is particularly valuable in the synthesis of peptides that require specific stereochemistry, allowing for the creation of compounds with enhanced biological activity. Researchers have successfully employed this amino acid in the design of peptide-based drugs, contributing to advancements in targeted therapies and personalized medicine. With its robust properties and significant role in peptide chemistry, Fmoc-(2R,3S)-3-phenylisoserine stands out as a crucial component for innovative research and development.

Synonyms
(2R,3S-3-(Fmoc-amino)-2-hydroxy-3-phenyl-propanoic acid
CAS Number
252206-27-2
Purity
≥ 99% (HPLC)
Molecular Formula
C24H21NO5
Molecular Weight
403.43
MDL Number
MFCD02259497
PubChem ID
53398433
Melting Point
191-199 ºC
Appearance
Off-white powder
Optical Rotation
[a]D20 = + 15 ± 2 º (C=1 in 80% C2H5OH)
Conditions
Store at 0-8°C
General Information
Synonyms
(2R,3S-3-(Fmoc-amino)-2-hydroxy-3-phenyl-propanoic acid
CAS Number
252206-27-2
Purity
≥ 99% (HPLC)
Molecular Formula
C24H21NO5
Molecular Weight
403.43
MDL Number
MFCD02259497
PubChem ID
53398433
Melting Point
191-199 ºC
Appearance
Off-white powder
Optical Rotation
[a]D20 = + 15 ± 2 º (C=1 in 80% C2H5OH)
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-(2R,3S)-3-phenylisoserine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for selective reactions without interfering with other functional groups. Its stability under various conditions makes it a preferred choice among chemists.
  • Drug Development: Researchers use it in the design of novel pharmaceuticals, particularly in creating compounds that target specific biological pathways, enhancing the efficacy of drug candidates.
  • Biotechnology: In the field of biotechnology, it aids in the development of therapeutic proteins and enzymes, contributing to advancements in treatments for various diseases.
  • Research in Neuroscience: The compound is utilized in studies related to neurobiology, helping to understand the role of amino acids in neurotransmission and potential implications in neurodegenerative diseases.
  • Custom Synthesis: Its unique structure allows for tailored modifications, making it valuable for custom synthesis projects in academic and industrial laboratories, addressing specific research needs efficiently.

Citations