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Catalog Number:
07346
CAS Number:
269078-71-9
Fmoc-(2S,4S-4-phenylpyrrolidine-2-carboxylic acid
Purity:
≥ 98% (HPLC)
Documents
$100.05 /100MG
Pack Size Availability Price
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Product Information

Fmoc-(2S,4S)-4-phenylpyrrolidine-2-carboxylic acid is a versatile compound widely utilized in the field of peptide synthesis and drug development. This compound serves as a protective group for amino acids, particularly in the synthesis of complex peptides, allowing for selective reactions without interference from other functional groups. Its unique structure, featuring a fluorenylmethoxycarbonyl (Fmoc) moiety, enhances stability and solubility, making it an ideal choice for researchers aiming to streamline their synthetic processes.

In addition to its role in peptide chemistry, Fmoc-(2S,4S)-4-phenylpyrrolidine-2-carboxylic acid is also valuable in medicinal chemistry for the development of bioactive compounds. Its ability to facilitate the formation of peptide bonds while maintaining the integrity of sensitive functional groups makes it a preferred choice among professionals in pharmaceutical research. The compound's high purity and reliability further contribute to its appeal, ensuring consistent results in various applications.

CAS Number
269078-71-9
Purity
≥ 98% (HPLC)
Molecular Formula
C26H23NO4
Molecular Weight
413.45
MDL Number
MFCD01074697
PubChem ID
4712574
Appearance
White powder
Optical Rotation
[a]20D = -42.4 ± 2 ° (C=1 in CHCl3
Conditions
Store at 0 - 8 °C
General Information
CAS Number
269078-71-9
Purity
≥ 98% (HPLC)
Molecular Formula
C26H23NO4
Molecular Weight
413.45
MDL Number
MFCD01074697
PubChem ID
4712574
Appearance
White powder
Optical Rotation
[a]20D = -42.4 ± 2 ° (C=1 in CHCl3
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

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

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: Its unique structure aids in the design of novel pharmaceuticals, particularly in creating compounds with enhanced bioactivity and selectivity for specific biological targets.
  • Bioconjugation: It is used in the conjugation of biomolecules, facilitating the attachment of drugs or imaging agents to proteins, which is crucial for targeted therapy and diagnostics.
  • Material Science: The compound is explored in the development of advanced materials, such as hydrogels and nanomaterials, which have applications in drug delivery systems and tissue engineering.
  • Research in Neuroscience: Its derivatives are investigated for their potential effects on neurotransmitter systems, contributing to the understanding of neurological disorders and the development of new treatments.

Citations