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Catalog Number:
15073
CAS Number:
359586-64-4
Fmoc-(1S,2S)-2-aminocyclopentane carboxylic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
(1S,2S)-Fmoc-Acpc
Documents
$113.87 /100MG
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Product Information

Fmoc-(1S,2S)-2-aminocyclopentane carboxylic acid is a versatile building block widely utilized in peptide synthesis and medicinal chemistry. This compound features the Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which is essential for the selective protection of amines during the synthesis of complex peptides. Its unique cyclopentane structure enhances the conformational flexibility of peptides, making it an ideal candidate for the development of bioactive compounds and pharmaceuticals. Researchers appreciate its ability to facilitate the introduction of cyclic structures into peptide chains, which can significantly improve the stability and efficacy of therapeutic agents.

In addition to its applications in peptide synthesis, Fmoc-(1S,2S)-2-aminocyclopentane carboxylic acid is also valuable in the design of novel ligands and inhibitors in drug discovery. Its distinctive properties allow for the exploration of new chemical spaces, potentially leading to the discovery of innovative treatments for various diseases. With its proven track record in enhancing peptide design and drug development, this compound stands out as a crucial tool for researchers and industry professionals aiming to advance their projects.

Synonyms
(1S,2S)-Fmoc-Acpc
CAS Number
359586-64-4
Purity
≥ 98% (HPLC)
Molecular Formula
C21H21NO4
Molecular Weight
351.4
MDL Number
MFCD04112694
PubChem ID
4712584
Appearance
White solid
Optical Rotation
[a]D25 = 35 ± 3 º (C=1 in MeOH)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
(1S,2S)-Fmoc-Acpc
CAS Number
359586-64-4
Purity
≥ 98% (HPLC)
Molecular Formula
C21H21NO4
Molecular Weight
351.4
MDL Number
MFCD04112694
PubChem ID
4712584
Appearance
White solid
Optical Rotation
[a]D25 = 35 ± 3 º (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-(1S,2S)-2-aminocyclopentane carboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, enhancing the efficiency of creating complex peptides by preventing unwanted reactions.
  • Drug Development: It plays a crucial role in the design of peptide-based pharmaceuticals, particularly in developing drugs targeting specific receptors due to its unique structural properties.
  • Bioconjugation: The compound is used in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, which is essential in creating targeted drug delivery systems.
  • Research in Neuroscience: It is utilized in studies related to neuropeptides, helping scientists understand their role in neurological functions and potential therapeutic applications.
  • Material Science: The compound can be incorporated into polymeric materials, enhancing their properties for applications in drug delivery systems and tissue engineering.

Citations