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Catalog Number:
15282
CAS Number:
269396-68-1
Boc-(4-pyridyl)-D-β-homoalanine
Purity:
≥ 99 % (HPLC)
Synonym(s):
Boc-D-β-HomoAla(4-pyridyl)-OH, Acide boc-( R -3-amino-4-(4-pyridyl)butyrique
Documents
$115.00 /25 mg
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Product Information

Boc-(4-pyridyl)-D-b-homoalanine is a versatile amino acid derivative that plays a significant role in peptide synthesis and medicinal chemistry. This compound features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and facilitates its use in various chemical reactions. Its unique structure, characterized by a pyridine ring, allows for increased interaction in biological systems, making it an excellent candidate for drug development and research applications. Researchers utilize Boc-(4-pyridyl)-D-b-homoalanine in the synthesis of bioactive peptides, where it can contribute to the design of novel therapeutics targeting various diseases, including cancer and neurological disorders.

The compound's ability to form stable conjugates with other biomolecules enhances its potential in drug delivery systems and targeted therapies. Additionally, its favorable solubility and reactivity profile make it an attractive choice for chemists looking to explore new avenues in peptide-based drug design. With its broad applicability in both academic and industrial settings, Boc-(4-pyridyl)-D-b-homoalanine stands out as a valuable tool for researchers aiming to innovate in the field of medicinal chemistry.

Synonyms
Boc-D-β-HomoAla(4-pyridyl)-OH, Acide boc-( R -3-amino-4-(4-pyridyl)butyrique
CAS Number
269396-68-1
Purity
≥ 99 % (HPLC)
Molecular Formula
C14H20N2O4
Molecular Weight
280.32
MDL Number
MFCD01076287
PubChem ID
18379146
Melting Point
145 - 151 °C
Appearance
Poudre blanc cassé
Optical Rotation
[α] D 25 = +15 ± 2º (C=1 dans EtOH)
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Boc-D-β-HomoAla(4-pyridyl)-OH, Acide boc-( R -3-amino-4-(4-pyridyl)butyrique
CAS Number
269396-68-1
Purity
≥ 99 % (HPLC)
Molecular Formula
C14H20N2O4
Molecular Weight
280.32
MDL Number
MFCD01076287
PubChem ID
18379146
Melting Point
145 - 151 °C
Appearance
Poudre blanc cassé
Optical Rotation
[α] D 25 = +15 ± 2º (C=1 dans EtOH)
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-(4-pyridyl)-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 creating modified peptides that can enhance biological activity or stability.
  • Drug Development: Its unique structure allows researchers to explore new drug candidates, especially in the field of cancer research, where modifications can lead to improved efficacy and reduced side effects.
  • Bioconjugation: The compound can be used to create bioconjugates, linking drugs to targeting moieties, which can improve the delivery of therapeutics to specific cells or tissues.
  • Research in Neuroscience: Its pyridine ring structure is beneficial in studying neurotransmitter systems, potentially leading to advancements in treatments for neurological disorders.
  • Analytical Chemistry: Boc-(4-pyridyl)-D-b-homoalanine can be utilized as a standard in analytical methods, aiding in the quantification and characterization of similar compounds in various samples.

Citations