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Catalog Number:
22685
CAS Number:
959583-57-4
3S)-4-Fmoc-1-carboximetil-3-bencil-piperazin-2-ona
Purity:
≥ 99 % (HPLC)
Documents
$86.23 /25 mg
Tamaño
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Product Information

The compound (3S)-4-Fmoc-1-carboxymethyl-3-benzyl-piperazin-2-one is a versatile building block in peptide synthesis and medicinal chemistry. Its unique structure, featuring a fluorenylmethoxycarbonyl (Fmoc) protecting group, allows for selective deprotection during the synthesis of complex peptides, making it an invaluable tool for researchers in the field of drug development. This compound is particularly beneficial in the design of peptide-based therapeutics, where precise control over amino acid sequences is crucial.

Additionally, its benzyl substitution enhances solubility and stability, which are essential properties for various applications in pharmaceutical formulations. Researchers have utilized this compound in the synthesis of bioactive peptides, contributing to advancements in targeted therapies and drug delivery systems. The ability to easily manipulate its structure while maintaining stability makes (3S)-4-Fmoc-1-carboxymethyl-3-benzyl-piperazin-2-one a preferred choice for professionals aiming to innovate in peptide chemistry and related fields.

CAS Number
959583-57-4
Purity
≥ 99 % (HPLC)
Molecular Formula
C28H26N2O5
Molecular Weight
470.52
MDL Number
MFCD06656483
PubChem ID
4712612
Appearance
Polvo blanco
Optical Rotation
=+59 ± 2º (C=1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
959583-57-4
Purity
≥ 99 % (HPLC)
Molecular Formula
C28H26N2O5
Molecular Weight
470.52
MDL Number
MFCD06656483
PubChem ID
4712612
Appearance
Polvo blanco
Optical Rotation
=+59 ± 2º (C=1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(3S)-4-Fmoc-1-carboxymethyl-3-benzyl-piperazin-2-one is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: It plays a crucial role in the development of pharmaceutical compounds, particularly in enhancing the solubility and stability of drug candidates.
  • Bioconjugation: The chemical is used in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other molecules, which is vital in creating targeted therapies.
  • Research in Neuroscience: It is employed in the synthesis of compounds that can modulate neurotransmitter systems, aiding in the study of neurological disorders.
  • Analytical Chemistry: This compound can be utilized in various analytical techniques, including chromatography, to separate and identify complex mixtures of substances.

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