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Catalog Number:
29689
CAS Number:
1313390-76-9
2S,4R-Fmoc-4-phenoxy-pyrrolidine-2-carboxylic acid
Purity:
≥ 98% (HPLC)
Documents
$100.05 /25MG
Pack Size Availability Price
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Product Information

The compound (2S,4R)-Fmoc-4-phenoxy-pyrrolidine-2-carboxylic acid is a versatile building block widely utilized in peptide synthesis and medicinal chemistry. Its unique structure, featuring a fluorenylmethoxycarbonyl (Fmoc) protecting group, allows for efficient and selective reactions, making it an ideal choice for researchers focused on developing complex peptides and pharmaceutical compounds. This compound's phenoxy group enhances its reactivity and solubility, facilitating its application in various organic synthesis processes.

In the pharmaceutical industry, (2S,4R)-Fmoc-4-phenoxy-pyrrolidine-2-carboxylic acid serves as a crucial intermediate in the synthesis of bioactive molecules, contributing to advancements in drug discovery and development. Its ability to stabilize peptide bonds and improve the overall yield of synthetic processes makes it a preferred choice among chemists. With its robust performance and reliability, this compound stands out as a valuable asset for both academic research and industrial applications.

CAS Number
1313390-76-9
Purity
≥ 98% (HPLC)
Molecular Formula
C26H23NO5
Molecular Weight
429.47
MDL Number
MFCD11226821
PubChem ID
53396277
Melting Point
63-82 ?C
Appearance
White powder
Optical Rotation
[a]D20 = -32 ± 2º (C=1 in MeOH)
Conditions
Store at 0-8 °C
General Information
CAS Number
1313390-76-9
Purity
≥ 98% (HPLC)
Molecular Formula
C26H23NO5
Molecular Weight
429.47
MDL Number
MFCD11226821
PubChem ID
53396277
Melting Point
63-82 ?C
Appearance
White powder
Optical Rotation
[a]D20 = -32 ± 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

(2S,4R)-Fmoc-4-phenoxy-pyrrolidine-2-carboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for the selective modification of amino acids during the assembly process, which is crucial in drug development.
  • Medicinal Chemistry: It plays a significant role in the design of novel pharmaceuticals, particularly in creating compounds with enhanced bioactivity and selectivity, aiding researchers in developing targeted therapies.
  • Bioconjugation: The chemical is used to facilitate the attachment of biomolecules to surfaces or other molecules, which is essential in creating effective drug delivery systems and diagnostic tools.
  • Research in Neuroscience: It is involved in the synthesis of compounds that can modulate neurotransmitter activity, providing insights into neurological disorders and potential treatments.
  • Material Science: This compound can be utilized in the development of advanced materials, such as polymers and nanomaterials, enhancing properties like strength and thermal stability for various industrial applications.

Citations