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Catalog Number:
30537
CAS Number:
1272754-91-2
2S,3S-(Fmoc-amino)-3-allyloxycarbonyl-aminobutyric acid
Purity:
≥ 99% (Assay by titration)
Synonym(s):
Fmoc-L-Abu(3S-Alloc-amino)-OH
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$154.93 /25MG
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Product Information

(2S,3S)-(Fmoc-amino)-3-allyloxycarbonylaminobutyric acid is a versatile compound widely utilized in peptide synthesis and drug development. 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 structure allows for the incorporation of an allyloxycarbonyl group, enhancing its reactivity and making it a valuable intermediate in the production of complex peptides and bioactive molecules. Researchers and industry professionals appreciate its role in facilitating the synthesis of therapeutic peptides, particularly in the fields of pharmaceuticals and biotechnology.

The compound's stability under various conditions and compatibility with standard coupling reagents make it an ideal choice for both academic research and industrial applications. Its ability to streamline the synthesis process while maintaining high purity levels is a significant advantage over similar compounds. With its practical applications in drug discovery and development, (2S,3S)-(Fmoc-amino)-3-allyloxycarbonylaminobutyric acid stands out as a crucial tool for chemists aiming to innovate in peptide-based therapies.

Synonyms
Fmoc-L-Abu(3S-Alloc-amino)-OH
CAS Number
1272754-91-2
Purity
≥ 99% (Assay by titration)
Molecular Formula
C23H24N2O6
Molecular Weight
424.4
MDL Number
MFCD07366900
PubChem ID
75627324
Melting Point
192 - 194 ?C
Appearance
White crystalline powder
Optical Rotation
[a]D20 = -23 ± 2 º (C=0.5 in DMF)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-L-Abu(3S-Alloc-amino)-OH
CAS Number
1272754-91-2
Purity
≥ 99% (Assay by titration)
Molecular Formula
C23H24N2O6
Molecular Weight
424.4
MDL Number
MFCD07366900
PubChem ID
75627324
Melting Point
192 - 194 ?C
Appearance
White crystalline powder
Optical Rotation
[a]D20 = -23 ± 2 º (C=0.5 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

(2S,3S)-(Fmoc-amino)-3-allyloxycarbonylaminobutyric acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create complex structures for drug development and biological studies.
  • Drug Development: Its unique functional groups enable the design of novel pharmaceuticals, particularly in targeting specific biological pathways, enhancing efficacy and reducing side effects.
  • Bioconjugation: The compound can be used to attach biomolecules to surfaces or other molecules, facilitating the development of targeted therapies and diagnostic tools in medicine.
  • Research in Organic Chemistry: It provides a versatile platform for exploring new reaction pathways and methodologies, contributing to advancements in synthetic organic chemistry.
  • Material Science: The compound's properties can be leveraged in creating advanced materials, such as drug delivery systems or smart polymers, enhancing their functionality and performance.

Citations