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Fmoc-L-beta-HVal-OH, a significant organic compound, holds great importance in the synthesis of peptides and proteins. This compound, derived from phenylalaninean essential amino acid, plays a role in the solid-phase peptide synthesis (SPPS) method. In the SPPS method, Fmoc-L-beta-HVal-OH serves as a valuable protecting group. By attaching the Fmoc group to the phenyl ring of phenylalanine, it effectively shields it from undesired reactions during the peptide synthesis process. This protective measure ensures that the intended modifications take place without any unwanted side effects. During the deprotection step, the Fmoc group is subsequently removed, facilitating the synthesis of the peptide. This deprotection exposes the phenyl ring, allowing further modifications to be made. Notably, the hydroxy group is added, expanding the possibilities for customizing and tailoring the peptide to specific requirements. The utilization of Fmoc-L-beta-HVal-OH in solid-phase peptide synthesis demonstrates its pivotal role in enabling the controlled and precise construction of peptides and proteins.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Fmoc-L-beta-HVal-OH, 1 g | sc-294878 | 1 g | $407.00 | |||
Fmoc-L-beta-HVal-OH, 5 g | sc-294878A | 5 g | $2040.00 |