Fmoc-3-Ala(3-benzothienyl)-OH

97%

  • Product Code: 50396
  CAS:    177966-60-8
Molecular Weight: 443.51 g./mol Molecular Formula: C₂₆H₂₁NO₄S
EC Number: MDL Number: MFCD00672562
Melting Point: Boiling Point: 690.8°C at 760 mmHg
Density: Storage Condition: 2-8°C, dry and sealed
Product Description: This chemical is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amino group during the synthesis process. The 3-benzothienyl side chain introduces a unique aromatic structure, which can be beneficial in designing peptides with specific biological activities or binding properties. It is commonly employed in the development of peptide-based drugs, research peptides, and biochemical studies where the incorporation of non-natural amino acids is required to enhance stability, activity, or selectivity. Its application is crucial in the synthesis of complex peptides for pharmaceutical and biotechnology industries.
Product Specification:
Test Specification
APPEARANCE White to pale cream Fused solid
PURITY 96.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days ฿1,740.00
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1.000 10-20 days ฿6,220.00
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5.000 10-20 days ฿27,990.00
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Fmoc-3-Ala(3-benzothienyl)-OH
This chemical is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amino group during the synthesis process. The 3-benzothienyl side chain introduces a unique aromatic structure, which can be beneficial in designing peptides with specific biological activities or binding properties. It is commonly employed in the development of peptide-based drugs, research peptides, and biochemical studies where the incorporation of non-natural amino acids is required to enhance stability, activity, or selectivity. Its application is crucial in the synthesis of complex peptides for pharmaceutical and biotechnology industries.
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