(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(anthracen-9-yl)propanoic acid

98%

  • Product Code: 50162
  CAS:    268734-27-6
Molecular Weight: 487.54 g./mol Molecular Formula: C₃₂H₂₅NO₄
EC Number: MDL Number: MFCD00671381
Melting Point: Boiling Point: 756.3±55.0°C at 760 mmHg
Density: Storage Condition: 2-8°C, dry and sealed
Product Description: This chemical is primarily utilized in peptide synthesis, particularly as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group serves as a protecting group for the amino functionality, allowing selective deprotection during solid-phase peptide synthesis. The anthracene moiety provides a unique fluorescent label, enabling the tracking and analysis of peptides during synthesis or in biochemical studies. This compound is valuable in research applications where precise control over peptide assembly and visualization is required, such as in the development of peptide-based drugs or fluorescent probes for biological systems. Its structure facilitates both synthetic flexibility and analytical monitoring in complex peptide synthesis workflows.
Product Specification:
Test Specification
APPEARANCE Yellow powder
PURITY 97.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿8,960.00
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0.250 10-20 days ฿16,680.00
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1.000 10-20 days ฿42,180.00
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(anthracen-9-yl)propanoic acid
This chemical is primarily utilized in peptide synthesis, particularly as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group serves as a protecting group for the amino functionality, allowing selective deprotection during solid-phase peptide synthesis. The anthracene moiety provides a unique fluorescent label, enabling the tracking and analysis of peptides during synthesis or in biochemical studies. This compound is valuable in research applications where precise control over peptide assembly and visualization is required, such as in the development of peptide-based drugs or fluorescent probes for biological systems. Its structure facilitates both synthetic flexibility and analytical monitoring in complex peptide synthesis workflows.
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