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Catalog Number:
16745
CAS Number:
220497-60-9
Ácido fmoc-L-2-amino-4-bromo-4-pentenoico
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-( S )-(2-bromoalil)glicina
Documents
$75.41 /100 mg
Tamaño
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Product Information

Fmoc-L-2-amino-4-bromo-4-pentenoic acid is a versatile building block widely utilized in peptide synthesis and medicinal chemistry. This compound features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which facilitates the selective deprotection of amino acids during solid-phase peptide synthesis. Its structure, characterized by the presence of a bromo group and a pentenoic acid moiety, enhances its reactivity and allows for the incorporation of diverse functionalities into peptides. Researchers appreciate its application in the development of bioactive peptides, which can be crucial for drug discovery and development.

In addition to its role in peptide synthesis, Fmoc-L-2-amino-4-bromo-4-pentenoic acid can be employed in the design of novel materials and therapeutic agents. Its unique properties make it an ideal candidate for studies in areas such as targeted drug delivery and the development of enzyme inhibitors. By leveraging its reactivity, chemists can create compounds with tailored properties for specific applications, making it a valuable asset in both academic and industrial settings.

Synonyms
Fmoc-( S )-(2-bromoalil)glicina
CAS Number
220497-60-9
Purity
≥ 98 % (HPLC)
Molecular Formula
C20H18BrNO4
Molecular Weight
416.27
MDL Number
MFCD01311750
PubChem ID
53397922
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
Safety & Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
General Information
Synonyms
Fmoc-( S )-(2-bromoalil)glicina
CAS Number
220497-60-9
Purity
≥ 98 % (HPLC)
Molecular Formula
C20H18BrNO4
Molecular Weight
416.27
MDL Number
MFCD01311750
PubChem ID
53397922
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
Safety & Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Properties
Additional property information coming soon!
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Applications

Fmoc-L-2-amino-4-bromo-4-pentenoic acid 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, allowing for the creation of complex and biologically active peptides.
  • Drug Development: It plays a significant role in the pharmaceutical industry for developing new drugs, especially those targeting specific proteins or enzymes, enhancing therapeutic efficacy.
  • Bioconjugation: The unique functional groups present facilitate bioconjugation processes, enabling researchers to attach biomolecules to surfaces or other molecules for targeted drug delivery systems.
  • Research in Neuroscience: This compound is used in studies related to neurotransmitter pathways, helping scientists understand the mechanisms of action in neurological disorders.
  • Material Science: Its properties are exploited in the development of novel materials, particularly in creating polymers with specific functionalities for various applications.

Citas