Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
22763
CAS Number:
352707-76-7
(+/-)-Fmoc- cis -ácido carboxílico 2-aminociclopentano
Purity:
≥ 96 % (HPLC)
Synonym(s):
Fmoc- cis -Acpc, Ácido carboxílico cis -2-aminociclopentano fmoc
Documents
$58.39 /250 mg
Tamaño
Request Bulk Quote
Product Information

(+/-)-Fmoc-cis-2-aminocyclopentane carboxylic acid is a versatile building block in peptide synthesis, particularly valued for its role in the development of peptide-based therapeutics and research applications. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is widely used in solid-phase peptide synthesis (SPPS) due to its stability and ease of removal under mild conditions. Its unique cis configuration allows for enhanced conformational flexibility, making it an ideal candidate for the synthesis of cyclic peptides and other complex structures. Researchers and industry professionals can leverage this compound to create novel peptides with specific biological activities, facilitating advancements in drug discovery and development.

The compound's properties, including its solubility and reactivity, further enhance its applicability in various chemical reactions, including coupling reactions and modifications. Its ability to provide a stable and easily removable protecting group makes it particularly advantageous compared to other amino acid derivatives. This compound is essential for those looking to innovate in peptide chemistry, offering a reliable option for synthesizing high-purity peptides with tailored functionalities.

Synonyms
Fmoc- cis -Acpc, Ácido carboxílico cis -2-aminociclopentano fmoc
CAS Number
352707-76-7
Purity
≥ 96 % (HPLC)
Molecular Formula
C21H21Nº 4
Molecular Weight
351.4
MDL Number
MFCD02682631
PubChem ID
4712584
Appearance
Polvo blanco o sólido de color crema.
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc- cis -Acpc, Ácido carboxílico cis -2-aminociclopentano fmoc
CAS Number
352707-76-7
Purity
≥ 96 % (HPLC)
Molecular Formula
C21H21Nº 4
Molecular Weight
351.4
MDL Number
MFCD02682631
PubChem ID
4712584
Appearance
Polvo blanco o sólido de color crema.
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(+/-)-Fmoc-cis-2-aminocyclopentane carboxylic acid 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. Its use enhances the efficiency of creating complex peptides, which are essential in drug development and biological research.
  • Drug Development: It plays a crucial role in the design of new pharmaceuticals, particularly in the development of cyclic peptides that can exhibit improved stability and bioactivity compared to linear peptides.
  • Bioconjugation: The compound is used in bioconjugation processes, where it helps link biomolecules to therapeutic agents, improving the targeting and efficacy of treatments in areas like cancer therapy.
  • Research in Neuroscience: Its structural properties make it valuable in studying neurotransmitter systems, aiding researchers in understanding how certain compounds interact with receptors in the brain.
  • Material Science: This chemical is also explored in the development of novel materials, particularly in creating polymers with specific properties for applications in drug delivery systems.

Citas