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Catalog Number:
15411
CAS Number:
270596-37-7
Fmoc-2-cloro-L-β-homofenilalanina
Purity:
≥ 99% (HPLC, pureza quiral)
Synonym(s):
Fmoc-L-β-HomoPhe(2-Cl)-OH, Ácido Fmoc-( S -3-amino-4-(2-clorofenil)butírico
Documents
$86.23 /100 mg
Tamaño
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Product Information

Fmoc-2-chloro-L-b-homophenylalanine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which facilitates the selective modification of amino acids during solid-phase peptide synthesis. Its chlorinated phenyl group enhances the compound's reactivity, making it an excellent choice for researchers looking to introduce specific functionalities into peptides.

In the pharmaceutical industry, Fmoc-2-chloro-L-b-homophenylalanine is particularly valuable for the development of peptide-based therapeutics, where precise control over peptide structure is crucial. Its application extends to the synthesis of bioactive peptides, which can be used in various therapeutic areas, including oncology and immunology. Researchers appreciate its ability to improve yields and purity in peptide synthesis, making it a preferred choice for both academic and industrial laboratories.

Synonyms
Fmoc-L-β-HomoPhe(2-Cl)-OH, Ácido Fmoc-( S -3-amino-4-(2-clorofenil)butírico
CAS Number
270596-37-7
Purity
≥ 99% (HPLC, pureza quiral)
Molecular Formula
C25H22ClNO4
Molecular Weight
435.91
MDL Number
MFCD01860997
PubChem ID
53397924
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-L-β-HomoPhe(2-Cl)-OH, Ácido Fmoc-( S -3-amino-4-(2-clorofenil)butírico
CAS Number
270596-37-7
Purity
≥ 99% (HPLC, pureza quiral)
Molecular Formula
C25H22ClNO4
Molecular Weight
435.91
MDL Number
MFCD01860997
PubChem ID
53397924
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 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-chloro-L-b-homophenylalanine 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 (SPPS), allowing for the creation of complex peptide sequences with high purity.
  • Drug Development: It is used in the development of novel therapeutic peptides, contributing to advancements in pharmaceuticals targeting specific diseases, including cancer and metabolic disorders.
  • Bioconjugation: The unique properties of this compound facilitate bioconjugation processes, enabling researchers to attach peptides to various biomolecules for targeted drug delivery systems.
  • Research in Neuroscience: Its applications extend to neuroscience, where it aids in the study of neuropeptides and their roles in neurological functions, potentially leading to breakthroughs in treatments for neurodegenerative diseases.
  • Custom Peptide Libraries: Researchers utilize this compound to create custom peptide libraries for high-throughput screening, which is essential for identifying new drug candidates and understanding protein interactions.

Citas