Date published: 2026-4-30

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Fmoc-L-beta-HVal-OH (CAS 172695-33-9)

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Alternate Names:
N-beta-(9-Fluorenylmethyloxycarbonyl)-L-homovaline
CAS Number:
172695-33-9
Molecular Weight:
353.41
Molecular Formula:
C21H23NO4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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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.


Fmoc-L-beta-HVal-OH (CAS 172695-33-9) References

  1. MCH-R1 Antagonist GPS18169, a Pseudopeptide, Is a Peripheral Anti-Obesity Agent in Mice.  |  Boutin, JA., et al. 2021. Molecules. 26: PMID: 33673598

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

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