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Catalog Number:
05750
CAS Number:
214750-77-3
Fmoc-4-(Boc-amino)-D-phenylalanine
Purity:
≥ 98%
Synonym(s):
Fmoc-D-Phe(4-NHBoc)-OH, Fmoc-p-(Boc-amino)-D-Phe-OH
Documents
$113.87 /1G
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Product Information

Fmoc-4-(Boc-amino)-D-phenylalanine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is crucial for the selective protection of amine functionalities during the synthesis of peptides. Its Boc (tert-butyloxycarbonyl) group further enhances its stability and solubility, making it an ideal choice for solid-phase peptide synthesis. Researchers and industry professionals appreciate its ability to facilitate the formation of complex peptide structures, which are vital in the development of therapeutic agents, particularly in the fields of oncology and immunology.

This compound stands out due to its unique combination of protective groups, allowing for greater control during synthesis and minimizing side reactions. Its applications extend to the production of peptide-based drugs, where precise amino acid sequences are critical for efficacy. Additionally, Fmoc-4-(Boc-amino)-D-phenylalanine can be employed in the study of protein interactions and the design of novel biomolecules, making it an essential tool for researchers in biochemistry and pharmaceutical sciences.

Synonyms
Fmoc-D-Phe(4-NHBoc)-OH, Fmoc-p-(Boc-amino)-D-Phe-OH
CAS Number
214750-77-3
Purity
≥ 98%
Molecular Formula
C29H30N2O6
Molecular Weight
502.6
MDL Number
MFCD00798642
PubChem ID
4712562
Appearance
White powder
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-D-Phe(4-NHBoc)-OH, Fmoc-p-(Boc-amino)-D-Phe-OH
CAS Number
214750-77-3
Purity
≥ 98%
Molecular Formula
C29H30N2O6
Molecular Weight
502.6
MDL Number
MFCD00798642
PubChem ID
4712562
Appearance
White powder
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-(Boc-amino)-D-phenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing for the introduction of protective groups that facilitate the assembly of complex peptide structures.
  • Drug Development: Its unique properties make it valuable in the pharmaceutical industry for developing new drugs, particularly those targeting specific biological pathways.
  • Bioconjugation: The compound is used in bioconjugation processes, which involve attaching biomolecules to other molecules, enhancing the efficacy of therapeutic agents.
  • Research in Neuroscience: It plays a role in studies related to neuropeptides, helping researchers understand their functions and potential therapeutic applications in neurological disorders.
  • Custom Peptide Libraries: The versatility of this compound allows for the creation of custom peptide libraries, which are essential for screening potential drug candidates and understanding protein interactions.

Citations