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Catalog Number:
07003
CAS Number:
142855-79-6
Fmoc-[3S]-3-amino-1-carboxymethylcaprolactame
Purity:
≥ 98% (HPLC)
Documents
$72.31 /100MG
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Product Information

Fmoc-[3S]-3-amino-1-carboxymethylcaprolactame is a versatile compound widely utilized in peptide synthesis and drug development. This amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amines 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 proteins. The compound's stability under various conditions enhances its applicability in both academic and industrial settings, particularly in the fields of pharmaceuticals and biotechnology.

In addition to its role in peptide synthesis, Fmoc-[3S]-3-amino-1-carboxymethylcaprolactame is also explored for its potential in developing novel therapeutics. Its ability to facilitate the formation of bioactive peptides positions it as a valuable tool for medicinal chemists aiming to create targeted therapies. With its favorable properties and practical applications, this compound stands out as a key ingredient in advancing research and development in peptide-based drug discovery.

CAS Number
142855-79-6
Purity
≥ 98% (HPLC)
Molecular Formula
C23H24N2O5
Molecular Weight
408.46
MDL Number
MFCD00270208
PubChem ID
4712603
Appearance
White powder
Optical Rotation
[a]20D = -6 ± 1 ° (C=1 in MeOH)
Conditions
Store at 0 - 8 °C
General Information
CAS Number
142855-79-6
Purity
≥ 98% (HPLC)
Molecular Formula
C23H24N2O5
Molecular Weight
408.46
MDL Number
MFCD00270208
PubChem ID
4712603
Appearance
White powder
Optical Rotation
[a]20D = -6 ± 1 ° (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-amino-1-carboxymethylcaprolactame is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: It plays a crucial role in the design of pharmaceutical compounds, particularly in the development of peptide-based drugs that can target specific biological pathways.
  • Bioconjugation: The compound is used in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules, which is essential in creating targeted therapies.
  • Research in Neuroscience: It is applied in studies involving neuropeptides, helping researchers understand the role of specific peptides in neurological functions and disorders.
  • Material Science: The compound is explored in the development of novel materials with tailored properties, particularly in creating biocompatible polymers for medical applications.