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Catalog Number:
29664
CAS Number:
1820570-42-0
Acide 2 R ,4 S -Boc-4-amino-1-Fmoc-pyrrolidine-2-carboxylique
Purity:
≥ 99 % (HPLC)
Documents
$65.40 /25 mg
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Product Information

The compound (2R,4S)-Boc-4-amino-1-Fmoc-pyrrolidine-2-carboxylic acid is a versatile building block in peptide synthesis and medicinal chemistry. This compound features a protected amino group and a carboxylic acid, making it an ideal candidate for the development of complex peptides and biologically active molecules. Its unique structure allows for selective reactions, which is crucial in the synthesis of pharmaceuticals and agrochemicals. Researchers appreciate its stability under various conditions, which enhances its utility in both laboratory and industrial settings.

In addition to its role in peptide synthesis, this compound can be utilized in the development of novel drug candidates, particularly in the fields of oncology and neurology. Its ability to facilitate the introduction of diverse functional groups makes it a valuable tool for medicinal chemists aiming to optimize drug efficacy and selectivity. The compound's favorable properties, such as solubility and reactivity, further support its application in high-throughput screening and lead optimization processes, making it a preferred choice for professionals in the pharmaceutical industry.

CAS Number
1820570-42-0
Purity
≥ 99 % (HPLC)
Molecular Formula
C25H28N2O6
Molecular Weight
452.51
MDL Number
MFCD12755471
PubChem ID
4712571
Appearance
Poudre blanche
Optical Rotation
[a] D 20 = +7 ± 2º (C = 1 dans DMF)
Conditions
Conserver à 0-8 °C
General Information
CAS Number
1820570-42-0
Purity
≥ 99 % (HPLC)
Molecular Formula
C25H28N2O6
Molecular Weight
452.51
MDL Number
MFCD12755471
PubChem ID
4712571
Appearance
Poudre blanche
Optical Rotation
[a] D 20 = +7 ± 2º (C = 1 dans DMF)
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

(2R,4S)-Boc-4-amino-1-Fmoc-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, allowing researchers to create complex structures for therapeutic applications.
  • Drug Development: It plays a significant role in the development of new pharmaceuticals, particularly in the design of drug candidates that target specific biological pathways.
  • Bioconjugation: The chemical is used in bioconjugation processes, where it helps to link biomolecules, enhancing the efficacy of targeted drug delivery systems.
  • Research in Neuroscience: It is applied in studies related to neurobiology, aiding in the development of compounds that can cross the blood-brain barrier for neurological treatments.
  • Custom Synthesis: This compound is favored for custom synthesis projects in academic and industrial labs, providing flexibility in creating tailored molecules for specific research needs.

Citations