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Catalog Number:
15404
CAS Number:
270263-07-5
Fmoc-(2-furil)-L-β-homoalanina
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-L-β-HomoAla(2-furil)-OH, Ácido Fmoc-( S -3-amino-4-(2-furil)butírico
Documents
$120.88 /25 mg
Tamaño
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Product Information

Fmoc-(2-furyl)-L-b-homoalanine is a versatile amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound features a unique furan ring, which enhances its reactivity and compatibility with various coupling reactions, making it an excellent choice for researchers in the fields of medicinal chemistry and biochemistry. Its Fmoc (fluorenylmethyloxycarbonyl) protecting group allows for easy deprotection under mild conditions, facilitating the synthesis of complex peptides and proteins.

This compound is particularly valuable in the development of peptide-based therapeutics, where the incorporation of furan-containing amino acids can impart desirable biological properties, such as increased stability and bioactivity. Researchers have utilized Fmoc-(2-furyl)-L-b-homoalanine in the design of novel peptide sequences aimed at targeting specific biological pathways, showcasing its potential in drug discovery and development. Its unique structure and properties make it a preferred choice for professionals seeking to innovate in peptide chemistry.

Synonyms
Fmoc-L-β-HomoAla(2-furil)-OH, Ácido Fmoc-( S -3-amino-4-(2-furil)butírico
CAS Number
270263-07-5
Purity
≥ 98 % (HPLC)
Molecular Formula
C23H21Nº 5
Molecular Weight
391.42
MDL Number
MFCD01861091
PubChem ID
53397999
Melting Point
139 - 145 °C
Appearance
Polvo de color blanco a blanquecino
Optical Rotation
[a] D 20 = -5 ± 1 º (C=1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-L-β-HomoAla(2-furil)-OH, Ácido Fmoc-( S -3-amino-4-(2-furil)butírico
CAS Number
270263-07-5
Purity
≥ 98 % (HPLC)
Molecular Formula
C23H21Nº 5
Molecular Weight
391.42
MDL Number
MFCD01861091
PubChem ID
53397999
Melting Point
139 - 145 °C
Appearance
Polvo de color blanco a blanquecino
Optical Rotation
[a] D 20 = -5 ± 1 º (C=1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-(2-furyl)-L-b-homoalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, allowing for the creation of complex peptide sequences with enhanced stability.
  • Drug Development: Its unique structure makes it a valuable candidate in the design of novel pharmaceuticals, especially those targeting specific biological pathways, due to its ability to mimic natural amino acids.
  • Bioconjugation: The compound can be used in bioconjugation processes, linking biomolecules such as proteins and antibodies to therapeutic agents, improving drug delivery and efficacy.
  • Research in Neuroscience: It has applications in neuroscience research, where it can be used to study neuropeptides and their roles in various neurological conditions, providing insights into potential treatments.
  • Material Science: Fmoc-(2-furyl)-L-b-homoalanine is also explored in the development of functional materials, particularly in creating hydrogels and nanomaterials with specific properties for biomedical applications.

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