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Catalog Number:
15743
CAS Number:
1217771-73-7
Fmoc-(S)-3-amino-3-(6-methoxy-3-pyridyl)propionic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-L-β-Ala-(6-methoxy-3-pyridyl)-OH
Documents
$65.40 /25MG
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Product Information

Fmoc-(S)-3-amino-3-(6-methoxy-3-pyridyl)propionic acid is a versatile building block 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. Its unique structure, characterized by the presence of a methoxy-substituted pyridine ring, enhances its solubility and reactivity, making it an ideal choice for researchers focused on developing complex peptide sequences.

In practical applications, this compound has been employed in the synthesis of bioactive peptides and pharmaceuticals, particularly in the development of targeted therapies and drug delivery systems. Its ability to facilitate the introduction of specific amino acid residues allows for the fine-tuning of peptide properties, which is crucial in optimizing therapeutic efficacy. Researchers in the fields of drug discovery and development will find this compound invaluable for its efficiency and effectiveness in producing high-purity peptides.

Synonyms
Fmoc-L-β-Ala-(6-methoxy-3-pyridyl)-OH
CAS Number
1217771-73-7
Purity
≥ 98% (HPLC)
Molecular Formula
C24H22N2O5
Molecular Weight
418.45
MDL Number
MFCD04118075
PubChem ID
53398102
Melting Point
211 - 213 °C
Appearance
White powder
Optical Rotation
[a]D25 = -28 ± 1 ° (C=1 in DMF)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-L-β-Ala-(6-methoxy-3-pyridyl)-OH
CAS Number
1217771-73-7
Purity
≥ 98% (HPLC)
Molecular Formula
C24H22N2O5
Molecular Weight
418.45
MDL Number
MFCD04118075
PubChem ID
53398102
Melting Point
211 - 213 °C
Appearance
White powder
Optical Rotation
[a]D25 = -28 ± 1 ° (C=1 in DMF)
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-(S)-3-amino-3-(6-methoxy-3-pyridyl)propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis (SPPS), allowing for the creation of complex peptide structures efficiently.
  • Drug Development: Its unique structure makes it valuable in the pharmaceutical industry for developing new drugs, especially those targeting neurological disorders, due to its ability to cross the blood-brain barrier.
  • Bioconjugation: The compound is used in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, enhancing the functionality of diagnostic tools and therapeutic agents.
  • Research in Neuroscience: It is applied in neuroscience research to study receptor interactions and signaling pathways, providing insights into brain function and potential treatments for cognitive disorders.
  • Analytical Chemistry: The compound is utilized in analytical methods to assess the purity and composition of complex mixtures, helping researchers ensure the quality of their chemical products.

Citations