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Catalog Number:
28559
CAS Number:
281655-37-6
S-4-N-Fmoc-3-morpholinecarboxylic acid
Purity:
≥ 99% (Chiral HPLC, HPLC)
Documents
$86.23 /25MG
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Product Information

(S)-4-N-Fmoc-3-morpholinecarboxylic acid is a versatile compound widely utilized in the field of peptide synthesis and drug development. This protected amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) group, which provides stability during the synthesis process while allowing for easy deprotection when needed. Its unique structure enhances solubility and reactivity, making it an ideal choice for researchers focused on developing complex peptides and biologically active molecules.

In addition to its applications in academic research, (S)-4-N-Fmoc-3-morpholinecarboxylic acid is also relevant in the pharmaceutical industry, where it can be employed in the design of novel therapeutics. Its ability to facilitate the formation of peptide bonds while maintaining the integrity of sensitive functional groups positions it as a valuable tool for chemists and biochemists alike. The compound's favorable properties, such as its stability and ease of use, make it a preferred choice for professionals seeking efficiency and reliability in their synthetic processes.

CAS Number
281655-37-6
Purity
≥ 99% (Chiral HPLC, HPLC)
Molecular Formula
C20H19NO5
Molecular Weight
353.37
MDL Number
MFCD01860732
PubChem ID
4461441
Appearance
Pale white solid
Optical Rotation
[a]D20 = -40.0 ± 2º (C=1 in MeOH)
Conditions
Store at 0-8 °C
General Information
CAS Number
281655-37-6
Purity
≥ 99% (Chiral HPLC, HPLC)
Molecular Formula
C20H19NO5
Molecular Weight
353.37
MDL Number
MFCD01860732
PubChem ID
4461441
Appearance
Pale white solid
Optical Rotation
[a]D20 = -40.0 ± 2º (C=1 in MeOH)
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

(S)-4-N-Fmoc-3-morpholinecarboxylic acid is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for selective reactions without interference from other functional groups.
  • Drug Development: It plays a crucial role in the design of pharmaceutical compounds, particularly in the development of biologically active molecules that target specific diseases.
  • Bioconjugation: The chemical is used in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other molecules, which is essential in creating targeted drug delivery systems.
  • Research in Organic Chemistry: It is a valuable reagent in organic synthesis, enabling chemists to explore new reaction pathways and develop innovative synthetic methodologies.
  • Material Science: The compound can be utilized in the development of advanced materials, including polymers and coatings, that require specific chemical functionalities for enhanced performance.

Citations