Fmoc-Tyr(3-Cl)-OH

≥95%

  • Product Code: 51117
  CAS:    478183-58-3
Molecular Weight: 437.87 g./mol Molecular Formula: C₂₄H₂₀ClNO₅
EC Number: MDL Number: MFCD02682261
Melting Point: Boiling Point: 674.9°C at 760 mmHg
Density: Storage Condition: 2-8°C, dry and sealed
Product Description: This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid building block, where the Fmoc group acts as a temporary protecting group for the amine functionality, ensuring selective peptide bond formation. The chlorine substituent on the tyrosine side chain provides unique properties, such as enhanced stability or altered reactivity, which can be beneficial in designing peptides with specific biological or structural characteristics. It is commonly employed in the development of peptides for pharmaceutical research, including drug discovery and the study of protein-protein interactions. Additionally, its modified tyrosine residue can be useful in creating peptides with tailored binding affinities or modified enzymatic activities.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days ฿882.00
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1.000 10-20 days ฿2,232.00
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5.000 10-20 days ฿7,029.00
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-
10.000 10-20 days ฿11,970.00
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-
Fmoc-Tyr(3-Cl)-OH
This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid building block, where the Fmoc group acts as a temporary protecting group for the amine functionality, ensuring selective peptide bond formation. The chlorine substituent on the tyrosine side chain provides unique properties, such as enhanced stability or altered reactivity, which can be beneficial in designing peptides with specific biological or structural characteristics. It is commonly employed in the development of peptides for pharmaceutical research, including drug discovery and the study of protein-protein interactions. Additionally, its modified tyrosine residue can be useful in creating peptides with tailored binding affinities or modified enzymatic activities.
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