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Catalog Number:
29686
CAS Number:
1579983-87-1
Acide Fmoc-trans-3-phényl-pyrrolidine-2-carboxylique racémique
Purity:
≥ 98 % (HPLC)
Documents
$100.00 /25 mg
Taille
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Product Information

Racemic Fmoc-trans-3-phenyl-pyrrolidine-2-carboxylic acid is a versatile compound widely utilized in the field of peptide synthesis and drug development. This compound serves as a crucial building block in the synthesis of various peptides, particularly in the creation of complex structures that require high specificity and stability. Its unique Fmoc (9-fluorenylmethyloxycarbonyl) protecting group allows for selective deprotection under mild conditions, making it an ideal choice for researchers aiming to streamline their synthetic processes.

In addition to its application in peptide synthesis, Racemic Fmoc-trans-3-phenyl-pyrrolidine-2-carboxylic acid has shown potential in medicinal chemistry, particularly in the design of novel pharmaceuticals targeting specific biological pathways. Its structural features contribute to enhanced bioactivity and selectivity, which are essential for developing effective therapeutic agents. Researchers and industry professionals can leverage this compound to facilitate advancements in drug discovery and development, ultimately leading to innovative solutions in healthcare.

CAS Number
1579983-87-1
Purity
≥ 98 % (HPLC)
Molecular Formula
C 26 H 234
Molecular Weight
413.47
MDL Number
MFCD35205371
PubChem ID
4712592
Appearance
Poudre blanche
Conditions
Conserver à 0 - 8 °C
General Information
CAS Number
1579983-87-1
Purity
≥ 98 % (HPLC)
Molecular Formula
C 26 H 234
Molecular Weight
413.47
MDL Number
MFCD35205371
PubChem ID
4712592
Appearance
Poudre blanche
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Racemic Fmoc-trans-3-phenyl-pyrrolidine-2-carboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: Its unique structure is beneficial in the design of new pharmaceuticals, particularly in creating compounds with improved bioactivity and stability.
  • Research in Neuroscience: The compound is used in studies related to neuroactive peptides, helping researchers understand their role in neurological processes and potential therapeutic applications.
  • Material Science: It can be incorporated into polymer systems to enhance properties such as thermal stability and mechanical strength, making it valuable in the development of advanced materials.
  • Analytical Chemistry: The compound is utilized in chromatography and other analytical techniques, aiding in the separation and identification of complex mixtures in various samples.

Citations