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Catalog Number:
15091
CAS Number:
959574-95-9
Fmoc-(S-3-amino-5-carboxymethyl-2,3-dihydro-1,5-benzoxazepin-4(5H)-one
Purity:
≥ 98.5% (HPLC)
Documents
$100.05 /25MG
Pack Size Availability Price
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Product Information

Fmoc-(S)-3-amino-5-carboxymethyl-2,3-dihydro-1,5-benzoxazepin-4(5H)-one is a versatile compound widely utilized in peptide synthesis and drug development. This compound features a unique benzoxazepin structure that enhances its stability and reactivity, making it an excellent choice for researchers focused on developing novel therapeutic agents. Its Fmoc (9-fluorenylmethoxycarbonyl) protecting group allows for easy incorporation into peptide chains, facilitating the synthesis of complex biomolecules.

In pharmaceutical research, this compound has shown promise in the development of targeted therapies due to its ability to modulate biological pathways effectively. Its carboxymethyl group contributes to its solubility in various solvents, making it suitable for diverse applications in medicinal chemistry and biochemistry. Researchers can leverage its properties to create innovative drug candidates, particularly in the fields of oncology and neurology, where precision and efficacy are paramount.

CAS Number
959574-95-9
Purity
≥ 98.5% (HPLC)
Molecular Formula
C26H22N2O6
Molecular Weight
458.47
MDL Number
MFCD04112700
PubChem ID
4712611
Appearance
White powder
Optical Rotation
[a]D20 = -170.6 ± 4º (C=1 in DMF)
Conditions
Store at 0-8 °C
General Information
CAS Number
959574-95-9
Purity
≥ 98.5% (HPLC)
Molecular Formula
C26H22N2O6
Molecular Weight
458.47
MDL Number
MFCD04112700
PubChem ID
4712611
Appearance
White powder
Optical Rotation
[a]D20 = -170.6 ± 4º (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-(S)-3-amino-5-carboxymethyl-2,3-dihydro-1,5-benzoxazepin-4(5H)-one is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: Its unique structure aids in the design of new pharmaceuticals, particularly in creating compounds that target specific biological pathways, enhancing efficacy and reducing side effects.
  • Bioconjugation: The chemical is used to attach biomolecules to surfaces or other molecules, which is crucial in developing targeted drug delivery systems and diagnostic tools.
  • Material Science: It contributes to the development of advanced materials, such as hydrogels and coatings, that require specific chemical properties for enhanced performance in various applications.
  • Research in Neuroscience: This compound is explored for its potential in studying neurological pathways and developing treatments for neurodegenerative diseases, thanks to its ability to cross the blood-brain barrier.

Citations