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Catalog Number:
07355
CAS Number:
209163-25-7
Fmoc-(R,S-3-1-carboxymethyl-2-valerolactame
Purity:
≥ 97% (HPLC)
Documents
$113.87 /100MG
Pack Size Availability Price
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Product Information

Fmoc-(R,S)-3-1-carboxymethyl-2-valerolactame is a versatile compound widely utilized in peptide synthesis and drug development. This compound features a unique Fmoc (fluorenylmethyloxycarbonyl) protecting group, which is essential for the selective protection of amino acids during the synthesis of peptides. Its structure allows for efficient coupling reactions, making it an ideal choice for researchers focused on developing complex peptide sequences. The compound's ability to stabilize reactive intermediates enhances its utility in various applications, including medicinal chemistry and biochemistry.

In addition to its role in peptide synthesis, Fmoc-(R,S)-3-1-carboxymethyl-2-valerolactame is also significant in the development of pharmaceuticals, particularly in creating compounds with improved bioavailability and efficacy. Its unique properties allow for the design of targeted drug delivery systems, making it a valuable asset in the pharmaceutical industry. Researchers and industry professionals can leverage this compound to streamline their synthesis processes and enhance the performance of their therapeutic candidates.

CAS Number
209163-25-7
Purity
≥ 97% (HPLC)
Molecular Formula
C22H22N2O5
Molecular Weight
394.44
MDL Number
MFCD03414134
PubChem ID
4712604
Appearance
White to off-white powder
Conditions
Store at 0-8°C
General Information
CAS Number
209163-25-7
Purity
≥ 97% (HPLC)
Molecular Formula
C22H22N2O5
Molecular Weight
394.44
MDL Number
MFCD03414134
PubChem ID
4712604
Appearance
White to off-white powder
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-(R,S)-3-1-carboxymethyl-2-valerolactame is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, allowing for the selective modification of amino acids while preventing unwanted reactions.
  • Drug Development: It plays a crucial role in the design of peptide-based therapeutics, particularly in optimizing the stability and bioavailability of drug candidates.
  • Bioconjugation: The chemical is used in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules, which is essential in creating targeted drug delivery systems.
  • Research on Neuroprotective Agents: It is being explored for its potential in developing neuroprotective agents, contributing to advancements in treating neurodegenerative diseases.
  • Analytical Chemistry: The compound is utilized in analytical methods for characterizing complex mixtures, aiding researchers in identifying and quantifying various substances in biological samples.

Citations