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Catalog Number:
29661
CAS Number:
1018332-24-5
Ácido (2 R ,4 R )-Fmoc-4-amino-1-Boc-pirrolidin-2-carboxílico
Purity:
≥ 99 % (HPLC)
Documents
$70.00 /25 mg
Tamaño
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Product Information

The compound (2R,4R)-Fmoc-4-amino-1-Boc-pyrrolidine-2-carboxylic acid is a versatile building block widely utilized in peptide synthesis and medicinal chemistry. Its unique structure, featuring both Fmoc and Boc protecting groups, allows for selective deprotection, making it an ideal choice for researchers focused on developing complex peptides and pharmaceuticals. This compound is particularly valuable in the synthesis of peptide-based drugs, where precise control over amino acid sequences is crucial.

In addition to its role in peptide synthesis, this compound can also be employed in the development of novel therapeutic agents, including those targeting various diseases. Its stability and compatibility with a range of reaction conditions enhance its appeal to professionals in the pharmaceutical and biotechnology sectors. Researchers appreciate its ability to facilitate the synthesis of bioactive compounds, thereby accelerating drug discovery processes. With its proven track record in the lab, (2R,4R)-Fmoc-4-amino-1-Boc-pyrrolidine-2-carboxylic acid stands out as a key reagent for innovative research and development.

CAS Number
1018332-24-5
Purity
≥ 99 % (HPLC)
Molecular Formula
C25H28N2O6
Molecular Weight
452.51
MDL Number
MFCD11519437
PubChem ID
3671690
Melting Point
160 - 167 °C (Literatura)
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D 20 = 20 ± 2 º (C=1 en DMF) D 20 = 18 ± 2 º (C=1 en MeOH)
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
1018332-24-5
Purity
≥ 99 % (HPLC)
Molecular Formula
C25H28N2O6
Molecular Weight
452.51
MDL Number
MFCD11519437
PubChem ID
3671690
Melting Point
160 - 167 °C (Literatura)
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D 20 = 20 ± 2 º (C=1 en DMF) D 20 = 18 ± 2 º (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

(2R,4R)-Fmoc-4-amino-1-Boc-pyrrolidine-2-carboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, enabling researchers to create complex molecules for drug development and therapeutic applications.
  • Drug Discovery: Its structural properties allow for modifications that can enhance the activity of potential drug candidates, making it valuable in pharmaceutical research.
  • Bioconjugation: The functional groups present facilitate bioconjugation processes, which are essential for developing targeted therapies and diagnostic agents in the biomedical field.
  • Research in Neuroscience: This compound can be used to study neuroactive peptides, contributing to a better understanding of neurological disorders and potential treatments.
  • Custom Synthesis: Due to its versatile reactivity, it is often employed in custom synthesis projects, allowing researchers to tailor compounds for specific applications in various scientific fields.

Citas