(R)-N-Fmoc-Α-(4-Pentynyl)Alanine

98%

  • Product Code: 231575
  CAS:    1198791-56-8
Molecular Weight: 391.46 g./mol Molecular Formula: C₂₄H₂₅NO₄
EC Number: MDL Number:
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Density: Storage Condition: Room temperature
Product Description: Widely used in peptide synthesis, this compound serves as a chiral building block for introducing alkyne functionality into peptide chains. The presence of the terminal alkyne allows for site-specific modification via click chemistry, particularly copper-catalyzed azide-alkyne cycloaddition (CuAAC). This is valuable in bioconjugation, enabling attachment of fluorophores, biotin, or other functional tags for detection, imaging, or immobilization. The Fmoc group ensures compatibility with standard solid-phase peptide synthesis (SPPS), allowing stepwise assembly under mild basic conditions. Its stereochemistry helps maintain desired peptide conformation, making it useful in the development of structured peptides, probes, and peptide-based therapeutics.
Sizes / Availability / Pricing:
Size Availability Price Quantity
0.100 10-20 days ฿16,840.00
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0.250 10-20 days ฿28,140.00
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1.000 10-20 days ฿76,750.00
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(R)-N-Fmoc-Α-(4-Pentynyl)Alanine
Widely used in peptide synthesis, this compound serves as a chiral building block for introducing alkyne functionality into peptide chains. The presence of the terminal alkyne allows for site-specific modification via click chemistry, particularly copper-catalyzed azide-alkyne cycloaddition (CuAAC). This is valuable in bioconjugation, enabling attachment of fluorophores, biotin, or other functional tags for detection, imaging, or immobilization. The Fmoc group ensures compatibility with standard solid-phase peptide synthesis (SPPS), allowing stepwise assembly under mild basic conditions. Its stereochemistry helps maintain desired peptide conformation, making it useful in the development of structured peptides, probes, and peptide-based therapeutics.
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