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Catalog Number:
15718
CAS Number:
1217736-81-6
Boc-(S-3-amino-3-(2-furyl)propionic acid
Purity:
≥ 98% (HPLC, Chiral purity)
Synonym(s):
Boc-D-β-Ala-(2-furyl)-OH
Documents
$72.31 /100MG
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Product Information

Boc-(S)-3-amino-3-(2-furyl)propionic acid is a valuable compound widely utilized in the field of organic synthesis and pharmaceutical research. This amino acid derivative features a furan ring, which enhances its reactivity and potential applications in the development of bioactive molecules. Its unique structure allows for the incorporation of the Boc (tert-butyloxycarbonyl) protecting group, making it an ideal candidate for peptide synthesis and modification. Researchers often leverage this compound in the design of novel therapeutics, particularly in the creation of peptide-based drugs that target specific biological pathways.

The compound's ability to facilitate the introduction of furan moieties into larger molecular frameworks opens up new avenues for drug discovery and development. Its applications extend to the synthesis of compounds with potential anti-inflammatory and anticancer properties, making it a critical tool for medicinal chemists. With its favorable properties and versatility, Boc-(S)-3-amino-3-(2-furyl)propionic acid stands out as a key ingredient in advancing pharmaceutical innovation and enhancing research outcomes.

Synonyms
Boc-D-β-Ala-(2-furyl)-OH
CAS Number
1217736-81-6
Purity
≥ 98% (HPLC, Chiral purity)
Molecular Formula
C12H17NO5
Molecular Weight
255.27
MDL Number
MFCD04117836
PubChem ID
24730273
Appearance
White powder
Optical Rotation
[a]D25 = -77 ± 2º (C=1 in MeOH)
Conditions
Store at 0-8 °C
General Information
Synonyms
Boc-D-β-Ala-(2-furyl)-OH
CAS Number
1217736-81-6
Purity
≥ 98% (HPLC, Chiral purity)
Molecular Formula
C12H17NO5
Molecular Weight
255.27
MDL Number
MFCD04117836
PubChem ID
24730273
Appearance
White powder
Optical Rotation
[a]D25 = -77 ± 2º (C=1 in MeOH)
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-(S)-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 development of pharmaceuticals targeting specific biological pathways.
  • Drug Development: Its unique structure allows for the design of novel drug candidates, especially in the field of neuropharmacology, where it can influence neurotransmitter activity.
  • Bioconjugation: The compound can be used in bioconjugation processes, linking biomolecules to therapeutic agents, enhancing the efficacy of targeted therapies.
  • Research on Amino Acid Analogues: It acts as an important model for studying amino acid analogues, contributing to the understanding of protein structure and function.
  • Material Science: In polymer chemistry, it can be incorporated into materials to improve properties such as biocompatibility and mechanical strength, making it useful for biomedical applications.

Citations