Boc-3-(1-naphthyl)-L-alanine

99%

  • Product Code: 104746
  Alias:    Boc-L-3-(1-naphthyl)-alanine ; N-tert-butoxycarbonyl-1-naphthyl-L-alanine
  CAS:    55447-00-2
Molecular Weight: 315.36 g./mol Molecular Formula: C₁₈H₂₁NO₄
EC Number: MDL Number: MFCD00085377
Melting Point: Boiling Point:
Density: Storage Condition: Room temperature, dry, sealed
Product Description: Boc-3-(1-naphthyl)-L-alanine is widely used in peptide synthesis as a protected amino acid derivative. Its Boc (tert-butyloxycarbonyl) group provides stability during the synthesis process, preventing unwanted reactions at the amino group. The naphthyl side chain introduces aromaticity and bulkiness, making it valuable in designing peptides with specific structural or functional properties. This compound is particularly useful in medicinal chemistry for developing peptide-based drugs, where the naphthyl group can enhance binding affinity to target proteins or receptors. Additionally, it is employed in research to study peptide conformation and interactions, aiding in the design of bioactive molecules. Its versatility makes it a key component in the synthesis of complex peptides for therapeutic and biochemical applications.
Product Specification:
Test Specification
Melting Point 142-146
Purity (HPLC) 99
Specific Rotation [A]20/D(C=1 In MeOH) -52.5--56.5
Appearance White To Light Yellow Powder
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days $27.00
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1.000 10-20 days $64.81
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5.000 10-20 days $218.42
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Boc-3-(1-naphthyl)-L-alanine
Boc-3-(1-naphthyl)-L-alanine is widely used in peptide synthesis as a protected amino acid derivative. Its Boc (tert-butyloxycarbonyl) group provides stability during the synthesis process, preventing unwanted reactions at the amino group. The naphthyl side chain introduces aromaticity and bulkiness, making it valuable in designing peptides with specific structural or functional properties. This compound is particularly useful in medicinal chemistry for developing peptide-based drugs, where the naphthyl group can enhance binding affinity to target proteins or receptors. Additionally, it is employed in research to study peptide conformation and interactions, aiding in the design of bioactive molecules. Its versatility makes it a key component in the synthesis of complex peptides for therapeutic and biochemical applications.
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