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Catalog Number:
04997
CAS Number:
160253-13-4
Fmoc-4-diethylphosphomethyl-L-phenylalanine
Purity:
≥ 99% (HPLC)
Synonym(s):
Fmoc-L-Phe(4-CH2PO3Et2)-OH
Documents
$58.39 /25MG
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Product Information

Fmoc-4-diethylphosphomethyl-L-phenylalanine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a unique phosphonate group that enhances its reactivity and stability, making it an ideal building block for the creation of complex peptides and proteins. Its Fmoc (fluorenylmethyloxycarbonyl) protecting group allows for easy incorporation into solid-phase peptide synthesis, facilitating the production of high-purity peptides that are crucial for pharmaceutical research and development.

Researchers and industry professionals can leverage Fmoc-4-diethylphosphomethyl-L-phenylalanine in various applications, including the design of peptide-based therapeutics and the study of protein interactions. Its ability to improve solubility and bioavailability compared to traditional amino acids makes it a valuable asset in the development of novel drug candidates. With its unique properties and practical applications, this compound stands out as a key ingredient in advancing peptide chemistry and biochemistry.

Synonyms
Fmoc-L-Phe(4-CH2PO3Et2)-OH
CAS Number
160253-13-4
Purity
≥ 99% (HPLC)
Molecular Formula
C29H32NO7P
Molecular Weight
537.56
MDL Number
MFCD01632024
PubChem ID
3457825
Appearance
White powder
Optical Rotation
C29H32NO7P
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-L-Phe(4-CH2PO3Et2)-OH
CAS Number
160253-13-4
Purity
≥ 99% (HPLC)
Molecular Formula
C29H32NO7P
Molecular Weight
537.56
MDL Number
MFCD01632024
PubChem ID
3457825
Appearance
White powder
Optical Rotation
C29H32NO7P
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-4-diethylphosphomethyl-L-phenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in solid-phase peptide synthesis, enabling researchers to create complex peptides with high purity and yield.
  • Drug Development: Its unique phosphonate group enhances the bioactivity of peptides, making it valuable in the design of new pharmaceuticals, particularly in targeting specific biological pathways.
  • Bioconjugation: The compound can be used to attach peptides to other biomolecules, facilitating the development of targeted drug delivery systems and improving therapeutic efficacy.
  • Research in Neuroscience: Due to its ability to modify peptide properties, it is employed in studies related to neuropeptides, aiding in the understanding of neurological functions and disorders.
  • Protein Engineering: The incorporation of this compound into proteins can enhance their stability and functionality, making it useful in the development of novel enzymes and therapeutic proteins.

Citations