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Catalog Number:
07420
CAS Number:
159611-02-6
Fmoc-β-(2-furil)-L-alanina
Purity:
≥ 99% (ensayo)
Synonym(s):
Fmoc-3-L-Ala(2-furil)-OH, Ácido ( S )-2-(Fmoc-amino)-3-(2-furil)propiónico
Documents
$149.02 /1G
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Product Information

Fmoc-b-(2-furyl)-L-alanine 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 provides distinct properties that are advantageous in various applications. Researchers appreciate its role in the synthesis of complex peptides, particularly in the development of pharmaceuticals where specificity and efficacy are crucial. The Fmoc protecting group allows for easy manipulation during synthesis, making it a preferred choice for chemists aiming to create high-purity peptides.

In addition to its applications in peptide synthesis, Fmoc-b-(2-furyl)-L-alanine has shown potential in medicinal chemistry, particularly in the design of bioactive compounds. Its structural characteristics lend themselves to the development of novel therapeutics targeting specific biological pathways. The compound's unique properties, combined with its ease of use, make it an essential tool for researchers and industry professionals focused on advancing drug discovery and development.

Synonyms
Fmoc-3-L-Ala(2-furil)-OH, Ácido ( S )-2-(Fmoc-amino)-3-(2-furil)propiónico
CAS Number
159611-02-6
Purity
≥ 99% (ensayo)
Molecular Formula
C 22 H 19 N.º 5
Molecular Weight
377.4
MDL Number
MFCD01311747
PubChem ID
4584639
Melting Point
123 - 126 °C (Literatura)
Appearance
Polvo de color blanco a blanquecino o ligeramente amarillento.
Optical Rotation
[a] D 20 = - 10 ± 2 °
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-3-L-Ala(2-furil)-OH, Ácido ( S )-2-(Fmoc-amino)-3-(2-furil)propiónico
CAS Number
159611-02-6
Purity
≥ 99% (ensayo)
Molecular Formula
C 22 H 19 N.º 5
Molecular Weight
377.4
MDL Number
MFCD01311747
PubChem ID
4584639
Melting Point
123 - 126 °C (Literatura)
Appearance
Polvo de color blanco a blanquecino o ligeramente amarillento.
Optical Rotation
[a] D 20 = - 10 ± 2 °
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-b-(2-furyl)-L-alanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create complex structures with specific functionalities.
  • Drug Development: Its unique properties make it valuable in the pharmaceutical industry for developing new drugs, particularly those targeting specific biological pathways.
  • Bioconjugation: The chemical is used in bioconjugation techniques, enabling the attachment of biomolecules to surfaces or other molecules, which is crucial in diagnostics and therapeutic applications.
  • Research in Organic Chemistry: It is employed in various organic synthesis reactions, providing chemists with a versatile tool for exploring new chemical reactions and pathways.
  • Material Science: The compound can be utilized in the development of novel materials, particularly in creating functionalized polymers that have applications in electronics and coatings.

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