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Catalog Number:
12632
CAS Number:
313052-02-7, 204058-25-3
N -α-Fmoc-β-(1-Boc-piperidin-4-il)-DL-alanina
Purity:
≥ 95 % (HPLC)
Synonym(s):
Ácido N -Fmoc-DL-amino-3-( N -Boc-4-piperidinil)propiónico
Documents
$134.70 /25 mg
Tamaño
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Product Information

N-a-Fmoc-b-(1-Boc-piperidin-4-yl)-DL-alanine is a versatile amino acid derivative widely utilized in peptide synthesis and medicinal chemistry. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. The presence of the Boc (tert-butyloxycarbonyl) group on the piperidine ring enhances its stability and solubility, making it an ideal choice for complex peptide constructions. Researchers and industry professionals appreciate its role in facilitating the synthesis of bioactive peptides and pharmaceuticals, particularly in the development of drug candidates targeting various biological pathways.

This compound's unique structure allows for efficient coupling reactions, which are crucial in the formation of peptide bonds. Its application extends to the synthesis of peptide-based therapeutics, where precise control over amino acid sequences is paramount. Moreover, N-a-Fmoc-b-(1-Boc-piperidin-4-yl)-DL-alanine stands out due to its compatibility with various coupling reagents, providing flexibility in synthetic methodologies. This makes it an invaluable tool for chemists aiming to innovate in peptide design and development.

Synonyms
Ácido N -Fmoc-DL-amino-3-( N -Boc-4-piperidinil)propiónico
CAS Number
313052-02-7, 204058-25-3
Purity
≥ 95 % (HPLC)
Molecular Formula
C28H34N2O6
Molecular Weight
494.6
MDL Number
MFCD01860501
PubChem ID
2734403
Appearance
Sólido de color blanco a blanquecino
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Ácido N -Fmoc-DL-amino-3-( N -Boc-4-piperidinil)propiónico
CAS Number
313052-02-7, 204058-25-3
Purity
≥ 95 % (HPLC)
Molecular Formula
C28H34N2O6
Molecular Weight
494.6
MDL Number
MFCD01860501
PubChem ID
2734403
Appearance
Sólido de color blanco a blanquecino
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

N-a-Fmoc-b-(1-Boc-piperidin-4-yl)-DL-alanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, which are essential in drug development and biological research.
  • Drug Design: It is employed in the design of novel pharmaceuticals, particularly in creating compounds that target specific biological pathways, enhancing therapeutic efficacy.
  • Bioconjugation: The chemical is useful in bioconjugation processes, allowing researchers to attach biomolecules to drugs or diagnostic agents, improving their specificity and effectiveness.
  • Research in Neuroscience: Its structural properties make it valuable in studying neuroactive compounds, aiding in the understanding of neurological disorders and potential treatments.
  • Custom Synthesis: The compound is often used in custom synthesis projects, providing flexibility for researchers to tailor molecules for specific applications in various fields.

Citas