Fmoc-S-3-amino-4-(4-methoxyphenyl)-butyric acid

98%

  • Product Code: 105148
  CAS:    1352435-52-9
Molecular Weight: 431.48 g./mol Molecular Formula: C₂₆H₂₅NO₅
EC Number: MDL Number: MFCD22887414
Melting Point: Boiling Point:
Density: Storage Condition: Room temperature, airtight, dry
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 amine functionality during the synthesis process. The presence of the 4-methoxyphenyl group in its structure makes it valuable for introducing specific aromatic and hydrophobic properties into peptide sequences, which can be crucial for studying peptide-protein interactions or designing bioactive peptides. Its application is prominent in pharmaceutical research, where it aids in the development of peptide-based drugs, enzyme inhibitors, and probes for biochemical studies. Additionally, it is utilized in the synthesis of modified peptides for exploring structure-activity relationships (SAR) in drug discovery.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days Ft21,623.63
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0.250 10-20 days Ft36,847.45
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1.000 10-20 days Ft77,864.48
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-
5.000 10-20 days Ft373,613.74
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Fmoc-S-3-amino-4-(4-methoxyphenyl)-butyric acid
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 amine functionality during the synthesis process. The presence of the 4-methoxyphenyl group in its structure makes it valuable for introducing specific aromatic and hydrophobic properties into peptide sequences, which can be crucial for studying peptide-protein interactions or designing bioactive peptides. Its application is prominent in pharmaceutical research, where it aids in the development of peptide-based drugs, enzyme inhibitors, and probes for biochemical studies. Additionally, it is utilized in the synthesis of modified peptides for exploring structure-activity relationships (SAR) in drug discovery.
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