(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-methyldec-9-enoic acid

95%

  • Product Code: 235009
  CAS:    288617-75-4
Molecular Weight: 421.53 g./mol Molecular Formula: C₂₆H₃₁NO₄
EC Number: MDL Number: MFCD12925760
Melting Point: 296°C Boiling Point: 647°C
Density: Storage Condition: Room temperature, dry
Product Description: Widely used in peptide synthesis, this compound serves as a protected amino acid derivative, enabling selective coupling reactions in solid-phase and solution-phase peptide assembly. The Fmoc group provides base-labile protection for the amine functionality, allowing orthogonal deprotection in the presence of other protecting groups. Its alkenyl side chain offers a site for further functionalization, such as cross-metathesis or click chemistry, making it valuable for introducing specific modifications in peptide chains. Commonly employed in the preparation of structured peptides, it supports the development of bioactive molecules, peptide conjugates, and peptidomimetics used in pharmaceutical research and drug design.
Sizes / Availability / Pricing:
Size Availability Price Quantity
0.050 10-20 days ฿1,990.00
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0.100 10-20 days ฿2,440.00
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1.000 10-20 days ฿12,270.00
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5.000 10-20 days ฿49,350.00
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0.250 10-20 days ฿4,560.00
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-methyldec-9-enoic acid
Widely used in peptide synthesis, this compound serves as a protected amino acid derivative, enabling selective coupling reactions in solid-phase and solution-phase peptide assembly. The Fmoc group provides base-labile protection for the amine functionality, allowing orthogonal deprotection in the presence of other protecting groups. Its alkenyl side chain offers a site for further functionalization, such as cross-metathesis or click chemistry, making it valuable for introducing specific modifications in peptide chains. Commonly employed in the preparation of structured peptides, it supports the development of bioactive molecules, peptide conjugates, and peptidomimetics used in pharmaceutical research and drug design.
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