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

Catalog Number:
15254
CAS Number:
220497-66-5
(+)-(1S,3R)-N-Fmoc-3-aminocyclopentane carboxylic acid
Purity:
≥ 95% (HPLC)
Synonym(s):
(+)-(1S,3R)-N-Fmoc-β-homocycloleucine
Documents
$154.93 /250MG
Pack Size Availability Price
Request Bulk Quote
Product Information

(+)-(1S,3R)-N-Fmoc-3-aminocyclopentane carboxylic acid is a versatile compound widely utilized in peptide synthesis and pharmaceutical research. This amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amines during the synthesis of peptides. Its unique cyclopentane structure enhances its stability and solubility, making it an excellent choice for researchers looking to develop novel peptides with improved bioactivity.

In the realm of medicinal chemistry, this compound serves as a critical building block for the development of bioactive peptides, which can be used in drug discovery and development. Its ability to facilitate the formation of complex peptide structures allows for the exploration of new therapeutic avenues, particularly in the fields of oncology and immunology. Researchers appreciate its ease of use and compatibility with various coupling reagents, making it a preferred choice for both academic and industrial applications.

Synonyms
(+)-(1S,3R)-N-Fmoc-β-homocycloleucine
CAS Number
220497-66-5
Purity
≥ 95% (HPLC)
Molecular Formula
C21H21NO4
Molecular Weight
351.4
MDL Number
MFCD01311757
PubChem ID
2734463
Appearance
White solid
Optical Rotation
[a]D20 = +13 ± 2º (C=1 in MeOH)
Conditions
Store at 0-8°C
General Information
Synonyms
(+)-(1S,3R)-N-Fmoc-β-homocycloleucine
CAS Number
220497-66-5
Purity
≥ 95% (HPLC)
Molecular Formula
C21H21NO4
Molecular Weight
351.4
MDL Number
MFCD01311757
PubChem ID
2734463
Appearance
White solid
Optical Rotation
[a]D20 = +13 ± 2º (C=1 in MeOH)
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(+)-(1S,3R)-N-Fmoc-3-aminocyclopentane carboxylic acid is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, allowing for the creation of complex peptide structures with high purity.
  • Drug Development: Its unique structure makes it valuable in the pharmaceutical industry for developing new drugs, especially those targeting specific receptors or pathways in the body.
  • Bioconjugation: The compound can be used in bioconjugation processes, linking biomolecules to other entities, enhancing the efficacy of therapeutic agents or diagnostic tools.
  • Research in Neuroscience: It is utilized in studies related to neurobiology, aiding in the exploration of new treatments for neurological disorders by modifying amino acid sequences in peptides.
  • Custom Chemical Synthesis: The compound's versatility allows researchers to tailor it for specific applications, making it a popular choice in custom synthesis projects across various fields.

Citations