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Catalog Number:
29764
CAS Number:
536747-87-2
Boc-4,4-Difluoro-D-proline
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$208.31 /100 mg
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Product Information

Boc-4,4-Difluoro-D-proline is a specialized amino acid derivative that plays a crucial role in the synthesis of peptide-based pharmaceuticals and research applications. This compound is characterized by its unique difluoro substitution, which enhances its stability and bioactivity compared to other proline derivatives. Researchers utilize Boc-4,4-Difluoro-D-proline in the development of novel therapeutic agents, particularly in the fields of medicinal chemistry and drug design. Its ability to serve as a building block in peptide synthesis allows for the creation of compounds with improved pharmacological properties, making it an invaluable tool for scientists aiming to innovate in drug development.

In addition to its applications in pharmaceuticals, Boc-4,4-Difluoro-D-proline is also employed in the study of protein folding and structure due to its distinctive conformational characteristics. Its incorporation into peptides can lead to enhanced binding affinity and selectivity, which are critical factors in the efficacy of therapeutic agents. This compound's unique properties not only facilitate advanced research but also provide significant advantages over traditional proline derivatives, making it a preferred choice for professionals in the field.

CAS Number
536747-87-2
Molecular Formula
C 10 H 15 F 2 NON 4
Molecular Weight
251.23
MDL Number
MFCD08272893
PubChem ID
23512514
Conditions
Conserver à 0-8°C
General Information
CAS Number
536747-87-2
Molecular Formula
C 10 H 15 F 2 NON 4
Molecular Weight
251.23
MDL Number
MFCD08272893
PubChem ID
23512514
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Boc-4,4-Difluoro-D-proline is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in the development of peptide-based drugs. Its unique difluorinated structure can enhance the stability and bioactivity of the resulting peptides.
  • Medicinal Chemistry: Researchers leverage its properties to design and optimize drug candidates, especially in the field of neuropharmacology, where modifications can lead to improved efficacy and reduced side effects.
  • Protein Engineering: It is used in the modification of amino acids within proteins, allowing scientists to study the effects of fluorination on protein structure and function, which can lead to breakthroughs in biochemistry.
  • Material Science: The compound finds applications in creating fluorinated polymers, which exhibit enhanced chemical resistance and thermal stability, making them suitable for advanced materials in various industries.
  • Research on Fluorinated Compounds: Its role in studying the effects of fluorine substitution on biological systems provides insights into the design of new fluorinated pharmaceuticals, offering potential advantages over non-fluorinated counterparts.

Citations