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Catalog Number:
04941
CAS Number:
176486-63-8
(2S,4R)-Fmoc-4-amino-1-Boc-pyrrolidine-2-carboxylic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-ABPC(2S,4R)-OH
Documents
$40.00 /250MG
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Product Information

The compound (2S,4R)-Fmoc-4-amino-1-Boc-pyrrolidine-2-carboxylic acid is a versatile building block widely utilized in peptide synthesis and medicinal chemistry. This compound features a protected amino group, making it ideal for the selective introduction of functional groups in complex organic molecules. Its unique structure allows for the efficient synthesis of peptides with high purity and yield, which is crucial in pharmaceutical development and research. Researchers appreciate its stability under various reaction conditions, enabling streamlined processes in the production of bioactive compounds.

In addition to its applications in peptide synthesis, this compound serves as a valuable intermediate in the development of novel therapeutics. Its ability to facilitate the formation of peptide bonds while maintaining the integrity of sensitive functional groups makes it a preferred choice among chemists. The Fmoc and Boc protecting groups provide flexibility in synthetic strategies, allowing for the sequential assembly of complex structures. This compound not only enhances the efficiency of synthetic routes but also contributes to the overall quality of the final products, making it an essential tool for professionals in the field.

Synonyms
Fmoc-ABPC(2S,4R)-OH
CAS Number
176486-63-8
Purity
≥ 98% (HPLC)
Molecular Formula
C25H28N2O6
Molecular Weight
452.51
MDL Number
MFCD00673783
PubChem ID
3671690
Appearance
White to off-white powder
Optical Rotation
[a]D20 = -15 ± 2 º (C=1 in MeOH)
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-ABPC(2S,4R)-OH
CAS Number
176486-63-8
Purity
≥ 98% (HPLC)
Molecular Formula
C25H28N2O6
Molecular Weight
452.51
MDL Number
MFCD00673783
PubChem ID
3671690
Appearance
White to off-white powder
Optical Rotation
[a]D20 = -15 ± 2 º (C=1 in MeOH)
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(2S,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, which are essential in drug development and biochemistry. Its protective groups allow for selective reactions, making it easier to create complex structures.
  • Drug Development: In pharmaceutical research, it is used to develop new therapeutic agents. Its unique structure can enhance the bioavailability and stability of drug candidates, leading to more effective medications.
  • Bioconjugation: The compound is employed in bioconjugation processes, linking biomolecules like proteins and antibodies to therapeutic agents. This application is crucial in creating targeted therapies for diseases such as cancer.
  • Research in Neuroscience: It plays a role in studies related to neuropeptides, which are vital for understanding brain function and developing treatments for neurological disorders.
  • Material Science: The compound is also explored in the development of novel materials, particularly in creating polymers that have specific functionalities, which can be used in various industrial applications.

Citations