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Catalog Number:
05027
CAS Number:
184700-26-3
Fmoc-(2S,6S,9S)-6-amino-2-carboxymethyl-3,8-diazabicyclo-(4,3,0)-nonane-1,4-dione
Purity:
≥ 97% (HPLC)
Synonym(s):
Fmoc-Acdn(2S,6S,9S)-OH
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$148.22 /100MG
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Product Information

Fmoc-(2S,6S,9S)-6-amino-2-carboxymethyl-3,8-diazabicyclo-(4,3,0)-nonane-1,4-dione is a specialized compound widely utilized in peptide synthesis and drug development. This compound features a unique bicyclic structure that enhances its stability and reactivity, making it an excellent choice for researchers focused on developing novel therapeutic agents. Its Fmoc (fluorenylmethyloxycarbonyl) protecting group allows for selective deprotection, facilitating the synthesis of complex peptides with high purity and yield.

In the pharmaceutical industry, this compound is particularly valuable for the synthesis of peptide-based drugs, where precise control over amino acid sequences is crucial. Its application extends to the development of targeted therapies and biologics, where the ability to manipulate peptide structures can lead to improved efficacy and reduced side effects. Researchers appreciate its compatibility with various coupling reagents and its ability to streamline the synthesis process, ultimately accelerating drug discovery and development timelines.

Synonyms
Fmoc-Acdn(2S,6S,9S)-OH
CAS Number
184700-26-3
Purity
≥ 97% (HPLC)
Molecular Formula
C24H23N3O6
Molecular Weight
449.46
MDL Number
MFCD01632025
PubChem ID
170999883
Appearance
White amorphous powder
Optical Rotation
[a]D = -60 ± 3º (C=1 in DMF)
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-Acdn(2S,6S,9S)-OH
CAS Number
184700-26-3
Purity
≥ 97% (HPLC)
Molecular Formula
C24H23N3O6
Molecular Weight
449.46
MDL Number
MFCD01632025
PubChem ID
170999883
Appearance
White amorphous powder
Optical Rotation
[a]D = -60 ± 3º (C=1 in DMF)
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-(2S,6S,9S)-6-amino-2-carboxymethyl-3,8-diazabicyclo-(4,3,0)-nonane-1,4-dione is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: It is used in the design of peptide-based drugs, particularly in the development of therapeutics targeting specific diseases, enhancing bioavailability and efficacy.
  • Bioconjugation: The chemical is valuable in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other compounds, which is crucial in diagnostics and therapeutic applications.
  • Research in Neuroscience: Its unique structure allows for the exploration of neuroactive peptides, aiding in the understanding of neurological pathways and potential treatments for neurological disorders.
  • Custom Synthesis: Researchers utilize this compound for custom synthesis projects, benefiting from its versatility in creating novel compounds for various applications in pharmaceuticals and materials science.

Citations