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Catalog Number:
15251
CAS Number:
219297-13-9
( S )-Boc-4-(4-pyridyl)-β-Homoala-OH
Purity:
≥ 99,5 % (HPLC chirale)
Synonym(s):
Boc-(4-pyridyl)-L-β-homoalanine, Acide boc-( S )-3-amino-4-(4-pyridyl)butyrique
Documents
$115.00 /25 mg
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Product Information

(S)-Boc-4-(4-pyridyl)-b-Homoala-OH is a versatile compound widely utilized in pharmaceutical research and development. This amino acid derivative features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and solubility, making it an ideal candidate for peptide synthesis and drug formulation. Its unique structure, characterized by the presence of a pyridine ring, contributes to its potential as a building block in the synthesis of bioactive molecules, particularly in the development of novel therapeutics targeting various diseases.

Researchers and industry professionals can leverage (S)-Boc-4-(4-pyridyl)-b-Homoala-OH in the creation of complex peptides and small molecules, facilitating advancements in medicinal chemistry. Its ability to serve as a chiral building block allows for the synthesis of enantiomerically pure compounds, which is crucial in the pharmaceutical industry for ensuring efficacy and safety in drug development. With its favorable properties and applications, this compound stands out as a valuable resource for those engaged in cutting-edge research and development.

Synonyms
Boc-(4-pyridyl)-L-β-homoalanine, Acide boc-( S )-3-amino-4-(4-pyridyl)butyrique
CAS Number
219297-13-9
Purity
≥ 99,5 % (HPLC chirale)
Molecular Formula
C14H20N2O4
Molecular Weight
280.32
MDL Number
MFCD01076288
PubChem ID
18379146
Appearance
Poudre jaune
Optical Rotation
[a] D 25 = -17,5 ± 2 º (C = 1 dans EtOH)
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Boc-(4-pyridyl)-L-β-homoalanine, Acide boc-( S )-3-amino-4-(4-pyridyl)butyrique
CAS Number
219297-13-9
Purity
≥ 99,5 % (HPLC chirale)
Molecular Formula
C14H20N2O4
Molecular Weight
280.32
MDL Number
MFCD01076288
PubChem ID
18379146
Appearance
Poudre jaune
Optical Rotation
[a] D 25 = -17,5 ± 2 º (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

(S)-Boc-4-(4-pyridyl)-b-Homoala-OH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for selective reactions without interfering with other functional groups. Its stability under various conditions makes it a preferred choice for chemists.
  • Drug Development: In pharmaceutical research, it is used in the design of novel compounds that target specific biological pathways, particularly in developing treatments for neurological disorders due to its pyridine structure.
  • Bioconjugation: The compound can be employed in bioconjugation strategies to attach biomolecules to surfaces or other molecules, enhancing the efficacy of drug delivery systems.
  • Material Science: Its properties allow for incorporation into polymers, leading to the development of materials with enhanced chemical resistance and thermal stability, beneficial in various industrial applications.
  • Analytical Chemistry: It is used as a standard in analytical methods such as HPLC, aiding in the quantification and characterization of related compounds in complex mixtures.

Citations