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Catalog Number:
07354
CAS Number:
215190-25-3
Fmoc-(3S-3-1-carboxymethyl-2-valerolactame
Purity:
≥ 97% (HPLC)
Documents
$194.99 /100MG
Pack Size Availability Price
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Product Information

Fmoc-(3S)-3-1-carboxymethyl-2-valerolactame is a versatile compound widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino acids during solid-phase peptide synthesis. Its unique structure allows for efficient coupling reactions, making it an ideal choice for researchers focused on synthesizing complex peptides and biologically active molecules. The compound's stability under various reaction conditions enhances its applicability in both academic and industrial settings, particularly in the pharmaceutical sector where precision and reliability are paramount.

In addition to its role in peptide synthesis, Fmoc-(3S)-3-1-carboxymethyl-2-valerolactame has shown potential in the development of novel therapeutics due to its ability to facilitate the formation of cyclic peptides. These cyclic structures often exhibit improved biological activity and stability compared to their linear counterparts. Researchers can leverage this compound to explore new avenues in drug discovery, particularly in the design of peptide-based drugs that target specific biological pathways. Its favorable properties and practical applications make it a valuable asset for professionals in the fields of chemistry and pharmaceuticals.

CAS Number
215190-25-3
Purity
≥ 97% (HPLC)
Molecular Formula
C22H22N2O5
Molecular Weight
394.44
MDL Number
MFCD02179648
PubChem ID
4712604
Appearance
White powder
Optical Rotation
[a]D = -13 ± 2º (C=1 in MeOH)
Conditions
Store at 0-8 °C
General Information
CAS Number
215190-25-3
Purity
≥ 97% (HPLC)
Molecular Formula
C22H22N2O5
Molecular Weight
394.44
MDL Number
MFCD02179648
PubChem ID
4712604
Appearance
White powder
Optical Rotation
[a]D = -13 ± 2º (C=1 in MeOH)
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-(3S)-3-1-carboxymethyl-2-valerolactame is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for the selective modification of amino acids without affecting others. This is crucial for researchers developing complex peptide-based drugs.
  • Drug Development: Its unique structure aids in the design of novel pharmaceuticals, particularly in creating compounds that can interact effectively with biological targets, enhancing therapeutic efficacy.
  • Bioconjugation: The chemical is used in bioconjugation processes, where it helps to attach biomolecules to drugs or imaging agents, improving their delivery and effectiveness in targeted therapies.
  • Material Science: In the development of advanced materials, it acts as a building block for creating functional polymers, which can be used in coatings, adhesives, and other applications requiring specific chemical properties.
  • Analytical Chemistry: This compound is employed in various analytical techniques, such as chromatography, to separate and analyze complex mixtures, providing valuable data for researchers in both academic and industrial settings.

Citations