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Catalog Number:
15403
CAS Number:
270263-06-4
Boc-(2-furyl)-L-β-homoalanine
Purity:
≥ 98% (HPLC)
Synonym(s):
Boc-L-β-HomoAla(2-furyl)-OH, Boc-(S)-3-amino-4-(2-furyl)butyric acid
Documents
$93.14 /25MG
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Product Information

Boc-(2-furyl)-L-b-homoalanine is a versatile amino acid derivative that plays a significant role in peptide synthesis and medicinal chemistry. This compound features a furan ring, which enhances its reactivity and allows for unique interactions in biological systems. Its Boc (tert-butyloxycarbonyl) protecting group provides stability during synthesis, making it an ideal choice for researchers focused on developing novel peptides and drug candidates. The compound's structural characteristics facilitate its use in the design of bioactive molecules, particularly in the fields of pharmaceuticals and biotechnology.

In practical applications, Boc-(2-furyl)-L-b-homoalanine is utilized in the synthesis of peptide-based therapeutics, where its unique properties can lead to improved efficacy and selectivity. Researchers have found that incorporating this compound into peptide sequences can enhance their biological activity, making it a valuable tool in drug discovery. Its compatibility with various coupling reagents and methodologies further supports its use in complex peptide synthesis, providing a reliable option for professionals aiming to innovate in the realm of peptide chemistry.

Synonyms
Boc-L-β-HomoAla(2-furyl)-OH, Boc-(S)-3-amino-4-(2-furyl)butyric acid
CAS Number
270263-06-4
Purity
≥ 98% (HPLC)
Molecular Formula
C13H19NO5
Molecular Weight
269.3
MDL Number
MFCD01861090
PubChem ID
53397998
Appearance
White to off-white powder
Optical Rotation
[a]D20 = +4 ± 2 º (C=1 in CHCl3)D25 = +4 ± 2º (C=1 in DMF)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Boc-L-β-HomoAla(2-furyl)-OH, Boc-(S)-3-amino-4-(2-furyl)butyric acid
CAS Number
270263-06-4
Purity
≥ 98% (HPLC)
Molecular Formula
C13H19NO5
Molecular Weight
269.3
MDL Number
MFCD01861090
PubChem ID
53397998
Appearance
White to off-white powder
Optical Rotation
[a]D20 = +4 ± 2 º (C=1 in CHCl3)D25 = +4 ± 2º (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

Boc-(2-furyl)-L-b-homoalanine 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 novel therapeutics targeting various diseases.
  • Drug Development: Its unique structure allows researchers to explore new drug candidates, especially in oncology and neurobiology, enhancing the efficacy of treatments.
  • Bioconjugation: The compound can be used in bioconjugation processes, linking biomolecules to improve drug delivery systems and targeted therapies.
  • Research in Neuroscience: Its furan ring structure is beneficial in studying neuroactive compounds, contributing to the understanding of neurotransmitter interactions.
  • Analytical Chemistry: Boc-(2-furyl)-L-b-homoalanine can be employed as a standard in analytical methods, aiding in the quantification of similar compounds in complex mixtures.

Citations