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Catalog Number:
14482
CAS Number:
959580-40-6
Ácido 2S , 4R -Fmoc-4-(4-bromobencil)pirrolidin-2-carboxílico
Purity:
≥ 98 % (HPLC)
Synonym(s):
(2 S , 4 R -Fmoc-4-(4-bromobencil)-Pro-OH
Documents
$134.70 /25 mg
Tamaño
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Product Information

The compound (2S,4R)-Fmoc-4-(4-bromobenzyl)pyrrolidine-2-carboxylic acid is a versatile building block widely utilized in peptide synthesis and medicinal chemistry. This compound features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which is crucial for the selective protection of amines during the synthesis of peptides. Its structural characteristics, including the bromobenzyl moiety, enhance its reactivity and compatibility with various coupling reactions, making it an ideal choice for researchers focused on developing complex peptide sequences.

In addition to its applications in peptide synthesis, this compound has shown potential in drug discovery and development, particularly in the design of bioactive molecules. The presence of the bromobenzyl group may contribute to improved binding affinity and selectivity in biological systems, which is essential for the development of effective therapeutics. Researchers and industry professionals can leverage this compound to streamline their synthesis processes while exploring innovative solutions in pharmaceutical applications.

Synonyms
(2 S , 4 R -Fmoc-4-(4-bromobencil)-Pro-OH
CAS Number
959580-40-6
Purity
≥ 98 % (HPLC)
Molecular Formula
C27H24NO4Br
Molecular Weight
506.4
MDL Number
MFCD06656467
PubChem ID
4712587
Appearance
Polvo blanco
Optical Rotation
[a] D 20 = -19 ± 2º (C=1 en CHCl 3 )
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
(2 S , 4 R -Fmoc-4-(4-bromobencil)-Pro-OH
CAS Number
959580-40-6
Purity
≥ 98 % (HPLC)
Molecular Formula
C27H24NO4Br
Molecular Weight
506.4
MDL Number
MFCD06656467
PubChem ID
4712587
Appearance
Polvo blanco
Optical Rotation
[a] D 20 = -19 ± 2º (C=1 en CHCl 3 )
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

(2S,4R)-Fmoc-4-(4-bromobenzyl)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, particularly in solid-phase peptide synthesis, allowing for the creation of complex peptide structures with high purity.
  • Drug Development: It plays a significant role in pharmaceutical research, particularly in the development of new drugs targeting specific biological pathways, enhancing the efficacy and selectivity of therapeutic agents.
  • Bioconjugation: The chemical is used in bioconjugation processes, where it helps attach biomolecules to drugs or imaging agents, improving their delivery and effectiveness in targeted therapies.
  • Research in Neuroscience: It is utilized in the synthesis of neuroactive compounds, contributing to studies on neurological disorders and the development of potential treatments.
  • Material Science: The compound is also explored in the development of novel materials, such as polymers and nanomaterials, which can have applications in electronics and drug delivery systems.

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