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Catalog Number:
15267
CAS Number:
268734-29-8
Fmoc-2-chloro-D-β-homophenylalanine
Synonym(s):
Fmoc-D-β-HomoPhe(2-Cl)-OH, Fmoc-(R-3-amino-4-(2-chlorophenyl)butyric acid
Documents
$86.23 /100MG
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Product Information

Fmoc-2-chloro-D-b-homophenylalanine is a valuable amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which enhances its stability and compatibility in solid-phase peptide synthesis. The presence of a chlorine atom on the phenyl ring provides additional reactivity, making it an ideal candidate for the synthesis of complex peptides and bioactive compounds. Researchers appreciate its ability to facilitate the introduction of diverse functionalities into peptide sequences, thereby expanding the scope of peptide-based therapeutics.

In practical applications, Fmoc-2-chloro-D-b-homophenylalanine has been employed in the development of peptide inhibitors, which play a crucial role in various biological processes. Its unique properties allow for the fine-tuning of peptide structures, enabling the design of molecules with enhanced efficacy and specificity. This compound is particularly relevant for researchers in medicinal chemistry and pharmaceutical development, as it supports the creation of innovative therapeutic agents with improved pharmacological profiles.

Synonyms
Fmoc-D-β-HomoPhe(2-Cl)-OH, Fmoc-(R-3-amino-4-(2-chlorophenyl)butyric acid
CAS Number
268734-29-8
Molecular Formula
C25H22ClNO4
Molecular Weight
435.91
MDL Number
MFCD01860899
PubChem ID
53397924
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-D-β-HomoPhe(2-Cl)-OH, Fmoc-(R-3-amino-4-(2-chlorophenyl)butyric acid
CAS Number
268734-29-8
Molecular Formula
C25H22ClNO4
Molecular Weight
435.91
MDL Number
MFCD01860899
PubChem ID
53397924
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-chloro-D-b-homophenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound is commonly used as a building block in solid-phase peptide synthesis, allowing researchers to create complex peptides efficiently.
  • Drug Development: Its unique structure makes it valuable in the design of novel pharmaceuticals, particularly in developing targeted therapies for various diseases.
  • Bioconjugation: The chemical is employed in bioconjugation processes, facilitating the attachment of biomolecules to drugs or diagnostics, enhancing their efficacy and specificity.
  • Research in Neuroscience: It serves as a tool in neuroscience research, helping to study receptor interactions and signaling pathways, which can lead to advancements in understanding neurological disorders.
  • Protein Engineering: The compound aids in the modification of proteins, allowing scientists to tailor their properties for specific applications in biotechnology and therapeutics.

Citations