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Catalog Number:
05031
CAS Number:
204326-24-9
Fmoc-(2S,5S)-5-amino-1,2,4,5,6,7-hexahydroazepino[3,2,1-H]indole-4-one-2-carboxylic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-Haic(2S,5S)-OH
Documents
$170.00 /25MG
Pack Size Availability Price
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Product Information

Fmoc-(2S,5S)-5-amino-1,2,4,5,6,7-hexahydroazepino[3,2,1-Hi]indole-4-one-2-carboxylic acid is a versatile compound widely utilized in peptide synthesis and drug development. This compound features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its structural characteristics enable efficient incorporation into various peptide sequences, making it a valuable tool for researchers in medicinal chemistry and biochemistry.

The compound's ability to facilitate the synthesis of complex peptides allows for the exploration of novel therapeutic agents, particularly in the fields of oncology and neurology. Additionally, its stability under standard reaction conditions enhances its appeal for use in automated peptide synthesizers. Researchers can leverage this compound to streamline their workflows and improve yields in peptide synthesis, ultimately advancing their projects with greater efficiency and precision.

Synonyms
Fmoc-Haic(2S,5S)-OH
CAS Number
204326-24-9
Purity
≥ 98% (HPLC)
Molecular Formula
C28H24N2O5
Molecular Weight
468.49
MDL Number
MFCD00673792
PubChem ID
4712606
Appearance
White powder
Optical Rotation
[a]25D = -117 ± 2 ° (C=1 in DMSO)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-Haic(2S,5S)-OH
CAS Number
204326-24-9
Purity
≥ 98% (HPLC)
Molecular Formula
C28H24N2O5
Molecular Weight
468.49
MDL Number
MFCD00673792
PubChem ID
4712606
Appearance
White powder
Optical Rotation
[a]25D = -117 ± 2 ° (C=1 in DMSO)
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,5S)-5-amino-1,2,4,5,6,7-hexahydroazepino[3,2,1-Hi]indole-4-one-2-carboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: Its unique structure makes it a valuable intermediate in the synthesis of bioactive compounds, particularly in developing pharmaceuticals targeting neurological disorders.
  • Bioconjugation: The chemical can be used to create bioconjugates, enhancing the delivery of therapeutic agents to specific cells, which is crucial in targeted drug delivery systems.
  • Research in Neuroscience: It is employed in studies investigating the mechanisms of action of neurotransmitters, aiding in the understanding of brain function and potential treatments for mental health disorders.
  • Analytical Chemistry: This compound can be utilized in the development of analytical methods for detecting and quantifying amino acids and peptides, providing essential tools for researchers in biochemistry.

Citations