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Catalog Number:
15398
CAS Number:
270263-01-9
Fmoc-(3-thienyl)-L-β-homoalanine
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-L-β-HomoAla(3-thienyl)-OH, Fmoc-(S-3-amino-4-(3-thienyl)butyric acid
Documents
$174.96 /100MG
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Product Information

Fmoc-(3-thienyl)-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 thienyl group, enhancing its properties for applications in medicinal chemistry and biochemistry. Its Fmoc (fluorenylmethyloxycarbonyl) protection allows for easy incorporation into peptide chains, making it an ideal choice for researchers focused on developing novel therapeutics. The compound's ability to participate in various coupling reactions expands its utility in the synthesis of complex peptides, which are essential in the development of biologically active compounds.

In addition to its applications in peptide synthesis, Fmoc-(3-thienyl)-L-b-homoalanine has shown potential in the design of bioactive molecules and as a building block in the creation of targeted drug delivery systems. Its unique structural features may contribute to improved binding affinities and selectivity in biological systems, making it a valuable asset for researchers in pharmaceutical and biochemical fields. With its combination of stability and reactivity, this compound is poised to support innovative research and development efforts.

Synonyms
Fmoc-L-β-HomoAla(3-thienyl)-OH, Fmoc-(S-3-amino-4-(3-thienyl)butyric acid
CAS Number
270263-01-9
Purity
≥ 98% (HPLC)
Molecular Formula
C23H21NO4S
Molecular Weight
407.48
MDL Number
MFCD01861085
PubChem ID
53397990
Melting Point
156-162 °C
Appearance
White powder
Optical Rotation
[a]D25 = -11 ± 1º (C=1 in DMF)
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-L-β-HomoAla(3-thienyl)-OH, Fmoc-(S-3-amino-4-(3-thienyl)butyric acid
CAS Number
270263-01-9
Purity
≥ 98% (HPLC)
Molecular Formula
C23H21NO4S
Molecular Weight
407.48
MDL Number
MFCD01861085
PubChem ID
53397990
Melting Point
156-162 °C
Appearance
White powder
Optical Rotation
[a]D25 = -11 ± 1º (C=1 in DMF)
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-(3-thienyl)-L-b-homoalanine 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 for various applications in drug development.
  • Drug Discovery: Its unique properties make it valuable in the pharmaceutical industry for designing novel compounds with potential therapeutic effects, particularly in targeting specific biological pathways.
  • Bioconjugation: The chemical can be used in bioconjugation processes, linking biomolecules to enhance drug delivery systems, improving the efficacy of therapeutic agents.
  • Material Science: In the field of materials, it can be incorporated into polymer systems to develop advanced materials with tailored properties for electronics or sensors.
  • Research on Protein Interactions: This compound aids in studying protein interactions and functions, providing insights that are crucial for understanding biological processes and disease mechanisms.

Citations