🌟 99% Happy customers

📦 Same-day shipping on in-stock items

Catalog Number:
15407
CAS Number:
270596-33-3
Boc-(2-furil)-D-β-homoalanina
Purity:
≥ 98 % (HPLC)
Synonym(s):
Boc-D-β-HomoAla(2-furil)-OH, Ácido Boc-( R -3-amino-4-(2-furil)butírico
Documents
$93.14 /25 mg
Tamaño
Request Bulk Quote
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-furil)-OH, Ácido Boc-( R -3-amino-4-(2-furil)butírico
CAS Number
270596-33-3
Purity
≥ 98 % (HPLC)
Molecular Formula
C 13 H 19 N.º 5
Molecular Weight
269.3
MDL Number
MFCD01860993
PubChem ID
53397998
Melting Point
104 - 110 °C
Appearance
Polvo de color blanco a blanquecino
Optical Rotation
[a] D 20 = -3 ± 2 º (C=1 en CHCl 3 )
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Boc-D-β-HomoAla(2-furil)-OH, Ácido Boc-( R -3-amino-4-(2-furil)butírico
CAS Number
270596-33-3
Purity
≥ 98 % (HPLC)
Molecular Formula
C 13 H 19 N.º 5
Molecular Weight
269.3
MDL Number
MFCD01860993
PubChem ID
53397998
Melting Point
104 - 110 °C
Appearance
Polvo de color blanco a blanquecino
Optical Rotation
[a] D 20 = -3 ± 2 º (C=1 en CHCl 3 )
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
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.

Citas