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Catalog Number:
15717
CAS Number:
1217725-33-1
Boc-(R-3-amino-3-(2-furyl)propionic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
Boc-L-β-Ala-(2-furyl)-OH
Documents
$75.41 /100MG
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Product Information

Boc-(R)-3-amino-3-(2-furyl)propionic acid is a versatile amino acid derivative that plays a crucial role in peptide synthesis and medicinal chemistry. This compound is particularly valued for its ability to introduce furan moieties into peptide structures, which can enhance biological activity and selectivity. Its Boc (tert-butyloxycarbonyl) protecting group allows for easy manipulation during chemical reactions, making it an ideal choice for researchers focused on developing novel therapeutics.

In pharmaceutical research, Boc-(R)-3-amino-3-(2-furyl)propionic acid is utilized in the design of bioactive peptides and can serve as a building block for more complex molecules. Its unique structure not only contributes to the stability of the resulting compounds but also opens avenues for the exploration of new drug candidates with improved efficacy. This compound is particularly relevant in the fields of drug discovery and development, where the incorporation of furan rings can lead to enhanced pharmacological properties.

Synonyms
Boc-L-β-Ala-(2-furyl)-OH
CAS Number
1217725-33-1
Purity
≥ 99% (HPLC)
Molecular Formula
C12H17NO5
Molecular Weight
255.27
MDL Number
MFCD04117839
PubChem ID
24730273
Melting Point
69-75 °C
Appearance
Off-white powder
Optical Rotation
[a]D25 = +72 ± 2º (C=1 in EtOH)
Conditions
Store at 0-8 °C
General Information
Synonyms
Boc-L-β-Ala-(2-furyl)-OH
CAS Number
1217725-33-1
Purity
≥ 99% (HPLC)
Molecular Formula
C12H17NO5
Molecular Weight
255.27
MDL Number
MFCD04117839
PubChem ID
24730273
Melting Point
69-75 °C
Appearance
Off-white powder
Optical Rotation
[a]D25 = +72 ± 2º (C=1 in EtOH)
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

Boc-(R)-3-amino-3-(2-furyl)propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in the pharmaceutical industry, where it can enhance the stability and bioactivity of peptide drugs.
  • Drug Development: Its unique structure allows researchers to explore novel drug candidates, especially in the development of treatments targeting neurological disorders, due to its ability to cross the blood-brain barrier.
  • Bioconjugation: The compound can be used in bioconjugation processes, linking biomolecules with therapeutic agents, which is crucial in creating targeted therapies for cancer treatment.
  • Research in Neuroscience: It is applied in studies related to neurotransmitter pathways, helping scientists understand the role of amino acids in brain function and the potential for new therapeutic interventions.
  • Analytical Chemistry: The compound is utilized in analytical methods to study amino acid interactions and behaviors, providing insights into protein structure and function.

Citations