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Catalog Number:
15407
CAS Number:
270596-33-3
Boc-(2-furyl)-D-β-homoalanine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Boc-D-β-HomoAla(2-furyl)-OH, Acide boc-( R -3-amino-4-(2-furyl)butyrique
Documents
$93.14 /25 mg
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Product Information

Boc-(2-furyl)-D-b-homoalanine is a versatile amino acid derivative that has garnered attention in the fields of medicinal chemistry and peptide synthesis. With its unique furan ring structure, this compound serves as an important building block for the development of bioactive peptides and pharmaceuticals. Its protective Boc (tert-butyloxycarbonyl) group enhances stability during synthesis, making it an ideal choice for researchers looking to create complex peptide sequences.

This compound is particularly valuable in the design of targeted therapies and drug candidates due to its ability to mimic natural amino acids while providing distinct functional properties. Its application extends to the synthesis of peptide-based drugs, where it can contribute to improved bioavailability and efficacy. Researchers can leverage Boc-(2-furyl)-D-b-homoalanine to explore novel therapeutic avenues, especially in oncology and neuropharmacology, where peptide therapeutics are increasingly being recognized for their potential.

Synonyms
Boc-D-β-HomoAla(2-furyl)-OH, Acide boc-( R -3-amino-4-(2-furyl)butyrique
CAS Number
270596-33-3
Purity
≥ 98 % (HPLC)
Molecular Formula
C 13 H 195
Molecular Weight
269.3
MDL Number
MFCD01860993
PubChem ID
53397998
Melting Point
104 - 110 °C
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] D 20 = -3 ± 2 º (C = 1 dans CHCl 3 )
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Boc-D-β-HomoAla(2-furyl)-OH, Acide boc-( R -3-amino-4-(2-furyl)butyrique
CAS Number
270596-33-3
Purity
≥ 98 % (HPLC)
Molecular Formula
C 13 H 195
Molecular Weight
269.3
MDL Number
MFCD01860993
PubChem ID
53397998
Melting Point
104 - 110 °C
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] D 20 = -3 ± 2 º (C = 1 dans CHCl 3 )
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Boc-(2-furyl)-D-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 bioactive compounds and pharmaceuticals.
  • Drug Development: Its unique structure allows for the creation of novel drug candidates, especially in the field of cancer research, where it can be used to design targeted therapies.
  • Bioconjugation: The compound can be employed in bioconjugation processes, linking biomolecules to enhance drug delivery systems or create diagnostic agents.
  • Research in Neuroscience: It is used in studies related to neuropeptides, helping researchers understand the role of specific amino acids in neurological functions.
  • Analytical Chemistry: Boc-(2-furyl)-D-b-homoalanine can be utilized as a standard in analytical methods, aiding in the quantification and characterization of similar compounds.

Citations