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Catalog Number:
22643
CAS Number:
321524-79-2
N-Fmoc-erythro-DL-β-methylphenylalanine
Purity:
≥ 98% (HPLC)
Synonym(s):
(2R,3R)/(2S,3S)-Fmoc-DL-β-methyl-Phe-OH, (2R,3R)/(2S,3S)-Racemic Fmoc-β-methyl-phenylalanine
Documents
$141.11 /100MG
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Product Information

N-Fmoc-erythro-DL-b-methylphenylalanine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc (9-fluorenylmethyloxycarbonyl) group, which enhances its stability and facilitates the formation of complex peptides. Its unique structure allows for selective reactions, making it an essential building block in the synthesis of bioactive peptides and pharmaceuticals. Researchers appreciate its ability to improve the solubility and bioavailability of peptide-based drugs, thereby enhancing therapeutic efficacy.

In addition to its applications in medicinal chemistry, N-Fmoc-erythro-DL-b-methylphenylalanine is also valuable in the development of novel materials and bioconjugates. Its compatibility with various coupling reagents and methodologies allows for streamlined synthesis processes, making it a preferred choice among chemists and researchers. By incorporating this compound into their workflows, professionals can achieve higher yields and purities in their peptide synthesis projects, ultimately leading to more effective therapeutic solutions.

Synonyms
(2R,3R)/(2S,3S)-Fmoc-DL-β-methyl-Phe-OH, (2R,3R)/(2S,3S)-Racemic Fmoc-β-methyl-phenylalanine
CAS Number
321524-79-2
Purity
≥ 98% (HPLC)
Molecular Formula
C25H23NO4
Molecular Weight
401.46
MDL Number
MFCD06656477
PubChem ID
3296415
Melting Point
151 - 156 °C
Appearance
White solid
Conditions
Store at 0 - 8 °C
General Information
Synonyms
(2R,3R)/(2S,3S)-Fmoc-DL-β-methyl-Phe-OH, (2R,3R)/(2S,3S)-Racemic Fmoc-β-methyl-phenylalanine
CAS Number
321524-79-2
Purity
≥ 98% (HPLC)
Molecular Formula
C25H23NO4
Molecular Weight
401.46
MDL Number
MFCD06656477
PubChem ID
3296415
Melting Point
151 - 156 °C
Appearance
White solid
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

N-Fmoc-erythro-DL-b-methylphenylalanine 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), allowing for the creation of complex peptide structures with high purity.
  • Drug Development: It is used in the development of pharmaceutical compounds, especially in the design of peptide-based drugs, enhancing their stability and bioavailability.
  • Bioconjugation: The chemical is valuable in bioconjugation processes, where it helps attach peptides to biomolecules, facilitating targeted drug delivery systems in cancer therapy.
  • Research in Neuroscience: It is applied in studies related to neurotransmitter systems, aiding researchers in understanding the role of specific peptides in neurological functions.
  • Protein Engineering: This compound is instrumental in protein engineering, allowing scientists to modify proteins for improved functionality, which is crucial in biotechnology applications.

Citations