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Catalog Number:
15408
CAS Number:
270596-34-4
Fmoc-(2-furyl)-D-β-homoalanine
Purity:
≥ 99% (HPLC)
Synonym(s):
Fmoc-(2-furyl)-D-β-homoalanine, Fmoc-R)-3-amino-4-(2-furyl)butyric acid
Documents
$154.93 /100MG
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Product Information

Fmoc-(2-furyl)-D-b-homoalanine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a unique furan ring, which enhances its reactivity and stability, making it an excellent choice for researchers looking to create complex peptide structures. Its Fmoc (fluorenylmethyloxycarbonyl) protecting group allows for easy incorporation into solid-phase peptide synthesis, facilitating the production of peptides with high purity and yield. Additionally, the presence of the furan moiety can impart distinct biological activities, making it a valuable building block in the design of novel therapeutics.

Researchers and industry professionals can leverage Fmoc-(2-furyl)-D-b-homoalanine in various applications, including the development of bioactive peptides and the exploration of new drug candidates. Its unique properties not only enhance the efficiency of peptide synthesis but also open avenues for innovative research in medicinal chemistry. With its ability to improve the pharmacological profile of peptides, this compound stands out as a crucial tool for advancing drug discovery and development.

Synonyms
Fmoc-(2-furyl)-D-β-homoalanine, Fmoc-R)-3-amino-4-(2-furyl)butyric acid
CAS Number
270596-34-4
Purity
≥ 99% (HPLC)
Molecular Formula
C23H21NO5
Molecular Weight
391.42
MDL Number
MFCD01860994
PubChem ID
53397999
Melting Point
139 - 145 °C
Appearance
White to off-white powder
Optical Rotation
[a]D20 = 4 ± 1 º (C=1 in DMF)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-(2-furyl)-D-β-homoalanine, Fmoc-R)-3-amino-4-(2-furyl)butyric acid
CAS Number
270596-34-4
Purity
≥ 99% (HPLC)
Molecular Formula
C23H21NO5
Molecular Weight
391.42
MDL Number
MFCD01860994
PubChem ID
53397999
Melting Point
139 - 145 °C
Appearance
White to off-white powder
Optical Rotation
[a]D20 = 4 ± 1 º (C=1 in DMF)
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-(2-furyl)-D-b-homoalanine 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, enhancing the efficiency and yield of complex peptide chains.
  • Drug Development: Its unique structure allows for the design of novel pharmaceutical compounds, especially in developing drugs targeting specific biological pathways, making it valuable in medicinal chemistry.
  • Bioconjugation: The functional groups in this compound facilitate bioconjugation processes, enabling the attachment of biomolecules to therapeutic agents, which is crucial in targeted drug delivery systems.
  • Research in Neuroscience: Its application in studying neuropeptides can help researchers understand neurological functions and disorders, providing insights for potential treatments.
  • Material Science: This compound can be incorporated into polymer matrices for creating advanced materials with specific properties, such as improved biocompatibility for medical devices.

Citations