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Catalog Number:
22733
CAS Number:
1361197-86-5
Ácido racémico Fmoc- trans -4-fenil-pirrolidin-3-carboxílico
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc- trans -DL-β-Pro-4-(fenil)-OH
Documents
$100.05 /25 mg
Tamaño
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Product Information

Racemic Fmoc-trans-4-phenyl-pyrrolidine-3-carboxylic acid is a versatile compound widely utilized in peptide synthesis and drug development. This compound features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which is essential for the selective protection of amines during the synthesis of peptides. Its trans configuration and the presence of a phenyl group enhance its stability and reactivity, making it an ideal choice for researchers looking to develop complex peptide structures.

In the pharmaceutical industry, this compound is particularly valuable for its role in the synthesis of bioactive peptides, which are crucial for therapeutic applications. Its ability to facilitate the formation of peptide bonds while maintaining the integrity of sensitive functional groups allows for the efficient production of peptides with high purity and yield. Additionally, Racemic Fmoc-trans-4-phenyl-pyrrolidine-3-carboxylic acid is recognized for its compatibility with various coupling reagents, further streamlining the synthesis process. This compound stands out for its reliability and effectiveness, making it a preferred choice for professionals in medicinal chemistry and biochemistry.

Synonyms
Fmoc- trans -DL-β-Pro-4-(fenil)-OH
CAS Number
1361197-86-5
Purity
≥ 99 % (HPLC)
Molecular Formula
C26H23NO4
Molecular Weight
413.47
MDL Number
MFCD09952615
PubChem ID
17040210
Melting Point
202-210 °C
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc- trans -DL-β-Pro-4-(fenil)-OH
CAS Number
1361197-86-5
Purity
≥ 99 % (HPLC)
Molecular Formula
C26H23NO4
Molecular Weight
413.47
MDL Number
MFCD09952615
PubChem ID
17040210
Melting Point
202-210 °C
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Racemic Fmoc-trans-4-phenyl-pyrrolidine-3-carboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in peptide synthesis, allowing for the selective modification of amino acids. Its stability under various conditions makes it a preferred choice for researchers in biochemistry.
  • Drug Development: The compound plays a crucial role in the design of pharmaceutical agents, particularly in the development of new drugs targeting neurological disorders. Its unique structure aids in enhancing the bioavailability of therapeutic compounds.
  • Material Science: It is used in the fabrication of advanced materials, including polymers and nanomaterials, due to its ability to influence the physical properties of the final product.
  • Bioconjugation: This chemical is instrumental in bioconjugation processes, where it helps in attaching biomolecules to surfaces or other molecules, enhancing the functionality of biosensors and diagnostic tools.
  • Research in Chiral Catalysis: The compound is utilized in studies related to chiral catalysis, providing insights into asymmetric synthesis, which is vital for producing enantiomerically pure compounds in various chemical industries.

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