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Catalog Number:
05019
CAS Number:
37535-57-2
Boc-3-(4'-pyridyl)-L-alanine
Purity:
≥ 99,5 % (HPLC chirale)
Synonym(s):
Boc-L-Ala(4'-pyridyl)-OH, Boc-β-(4'-pyridyl)-Ala-OH, Boc-β-(4'-pyridyl)-Ala-OH
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Product Information

Boc-3-(4'-pyridyl)-L-alanine is a versatile amino acid derivative that plays a significant role in peptide synthesis and drug development. This compound features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and solubility, making it an ideal choice for researchers in the fields of medicinal chemistry and biochemistry. Its unique structure, characterized by the pyridine ring, allows for specific interactions in biological systems, facilitating the design of targeted therapeutics.

In practical applications, Boc-3-(4'-pyridyl)-L-alanine is utilized in the synthesis of bioactive peptides and as a building block in the development of pharmaceuticals. Its ability to form stable linkages with other amino acids enhances the efficacy of drug candidates, particularly in the treatment of various diseases. Researchers appreciate its compatibility with standard coupling reagents and methodologies, streamlining the synthesis process while ensuring high yields. This compound not only supports innovative research but also holds potential for advancing therapeutic strategies in the pharmaceutical industry.

Synonyms
Boc-L-Ala(4'-pyridyl)-OH, Boc-β-(4'-pyridyl)-Ala-OH, Boc-β-(4'-pyridyl)-Ala-OH
CAS Number
37535-57-2
Purity
≥ 99,5 % (HPLC chirale)
Molecular Formula
C13H18N2O4
Molecular Weight
266.3
MDL Number
MFCD00672528
PubChem ID
3294373
Melting Point
224 - 232 ?C
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] 20 D = -30 ± 1 ° (C = 1 dans DMF)
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Boc-L-Ala(4'-pyridyl)-OH, Boc-β-(4'-pyridyl)-Ala-OH, Boc-β-(4'-pyridyl)-Ala-OH
CAS Number
37535-57-2
Purity
≥ 99,5 % (HPLC chirale)
Molecular Formula
C13H18N2O4
Molecular Weight
266.3
MDL Number
MFCD00672528
PubChem ID
3294373
Melting Point
224 - 232 ?C
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] 20 D = -30 ± 1 ° (C = 1 dans DMF)
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-3-(4'-pyridyl)-L-alanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in peptide synthesis, allowing for the selective modification of amino acids. Its stability under various reaction conditions makes it a preferred choice for chemists.
  • Drug Development: The compound's unique structure can be integrated into drug candidates, particularly in the development of pharmaceuticals targeting neurological disorders, leveraging its pyridine ring for enhanced receptor interactions.
  • Bioconjugation: It is employed in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other molecules, which is crucial in creating targeted therapies and diagnostics.
  • Research in Neuroscience: The compound's pyridine moiety is beneficial in studying neurotransmitter systems, making it valuable in academic and pharmaceutical research aimed at understanding brain function and disorders.
  • Analytical Chemistry: Boc-3-(4'-pyridyl)-L-alanine is used as a standard in analytical methods, aiding in the quantification and characterization of related compounds in complex mixtures.

Citations