Fmoc-D-Tyr(Bzl)-OH
98%
- Product Code: 76161
CAS:
138775-48-1
| Molecular Weight: | 493.55 g./mol | Molecular Formula: | C₃₁H₂₇NO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00235837 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, avoid light, store in inert gas |
Product Description:
Fmoc-D-Tyr(Bzl)-OH is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group protects the amino group, and the Bzl (benzyl) group protects the hydroxyl group of the tyrosine side chain. This protection is crucial for preventing unwanted side reactions during the stepwise assembly of peptides. Its application is essential in the production of complex peptides for pharmaceutical research, drug development, and biochemical studies. Additionally, it is used in the synthesis of peptide-based therapeutics, hormones, and enzyme inhibitors, where precise control over amino acid incorporation is required. Its stability and compatibility with SPPS protocols make it a valuable tool in peptide chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿720.00 |
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| 5.000 | 10-20 days | ฿2,502.00 |
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| 25.000 | 10-20 days | ฿8,505.00 |
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Fmoc-D-Tyr(Bzl)-OH
Fmoc-D-Tyr(Bzl)-OH is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group protects the amino group, and the Bzl (benzyl) group protects the hydroxyl group of the tyrosine side chain. This protection is crucial for preventing unwanted side reactions during the stepwise assembly of peptides. Its application is essential in the production of complex peptides for pharmaceutical research, drug development, and biochemical studies. Additionally, it is used in the synthesis of peptide-based therapeutics, hormones, and enzyme inhibitors, where precise control over amino acid incorporation is required. Its stability and compatibility with SPPS protocols make it a valuable tool in peptide chemistry.
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