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Catalog Number:
29688
CAS Number:
1260617-48-8
Ácido 2S , 4S -Fmoc-4-fenoxi-pirrolidin-2-carboxílico
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-L- cis -4-fenoxiprolina
Documents
$154.93 /100 mg
Tamaño
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Product Information

The compound (2S,4S)-Fmoc-4-phenoxy-pyrrolidine-2-carboxylic acid is a versatile building block widely utilized in peptide synthesis and medicinal chemistry. Known for its protective Fmoc (9-fluorenylmethoxycarbonyl) group, this compound facilitates the selective modification of amino acids, making it an essential tool for researchers in the field of organic synthesis. Its unique structure, featuring a phenoxy group, enhances its reactivity and compatibility with various coupling reactions, allowing for the efficient assembly of complex peptide sequences.

In addition to its role in peptide synthesis, this compound has potential applications in drug development, particularly in the design of bioactive peptides and pharmaceuticals. Its ability to stabilize peptide structures and improve solubility can lead to enhanced therapeutic efficacy. Researchers and industry professionals can leverage the advantages of (2S,4S)-Fmoc-4-phenoxy-pyrrolidine-2-carboxylic acid to streamline their synthesis processes and achieve higher yields in their projects.

Synonyms
Fmoc-L- cis -4-fenoxiprolina
CAS Number
1260617-48-8
Purity
≥ 98 % (HPLC)
Molecular Formula
C26H23NO5
Molecular Weight
429.47
MDL Number
MFCD11226822
PubChem ID
53396277
Appearance
Polvo blanco
Optical Rotation
[a] D 20 = -8 ± 1º (C=1 en MeOH)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-L- cis -4-fenoxiprolina
CAS Number
1260617-48-8
Purity
≥ 98 % (HPLC)
Molecular Formula
C26H23NO5
Molecular Weight
429.47
MDL Number
MFCD11226822
PubChem ID
53396277
Appearance
Polvo blanco
Optical Rotation
[a] D 20 = -8 ± 1º (C=1 en MeOH)
Conditions
Conservar entre 0 y 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,4S)-Fmoc-4-phenoxy-pyrrolidine-2-carboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, allowing for the creation of complex and diverse peptide structures.
  • Drug Development: Its unique structure makes it a candidate for designing new pharmaceuticals, especially in developing compounds that target specific biological pathways, enhancing therapeutic efficacy.
  • Bioconjugation: The compound can be used in bioconjugation techniques, linking biomolecules like proteins and antibodies to therapeutic agents, which is crucial in targeted drug delivery systems.
  • Research in Neuroscience: It plays a role in the synthesis of neuroactive compounds, aiding researchers in studying neurological disorders and developing potential treatments.
  • Material Science: This chemical can be incorporated into polymer systems, contributing to the development of advanced materials with specific properties for applications in coatings and drug delivery.

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